K&R TECHNOLOGIES DBA MICROBIOLOGY INTERNATIONAL

FDA Device Registration & Listing · Frederick, MD, US · Registration 3013823481

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013823481
FEI Number
3013823481
Entity Name
K&R TECHNOLOGIES DBA MICROBIOLOGY INTERNATIONAL
City/State/Country
Frederick, MD, US
Establishment Address
5350 Partners Ct, Suite A, Frederick, MD 21703, US
Establishment Type(s)
N/A
Owner / Operator
K&R Technologies dba Microbiology International (Owner Number: 10091040)
Owner / Operator Contact Address
5350 Partners Ct, Suite A, Frederick, MD 21703, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Whitley A55 Anaerobic Workstation Whitley A45 Anaerobic Workstation Whitley A25 Anaerobic Workstation Whitley A35 Anaerobic Workstation Whitley A95 Anaerobic Workstation Whitley A85 Anaerobic Workstation Whitley A155 HEPA Anaerobic Workstation Whitley A20 Anaerobic Workstation Whitley A135 HEPA Anaerobic Workstation COLOREX Orientation CHROMagar Orientation Whitley AtmoGen Jar Gassing System Whitley AtmoGen Jar Gassing System COLOREX Malassezia CHROMagar Liquid ECC COLOREX Candida CHROMagar Serratia COLOREX ECC CHROMagar Acinetobacter CHROMagar Campylobacter COLOREX Streptococcus COLOREX STEC CHROMagar VRE COLOREX Staph aureus CHROMagar Salmonella CHROMagar Staphylococcus CHROMagar Streptococcus COLOREX CCA CHROMagar Vibrio COLOREX Listeria CHROMagar C. difficile CHROMagar Mycoplasma COLOREX MRSA Rambach Agar CHROMagar B. cepacia COLOREX Mycoplasma CHROMagar B. cereus COLOREX ESBL CHROMagar Listeria CHROMagar Salmonella Plus RambaCHROM KPC CHROMagar C. perfringens COLOREX Strep A CHROMagar Pasteurella COLOREX LIN-R COLOREX Strep ACG CHROMagar TBX COLOREX B. cepacia COLOREX C. difficile CHROMagar O157 CHROMagar Strep B CHROMagar MRSA CHROMagar Cronobacter COLOREX Pasteurella COLOREX VRE CHROMagar E. coli CHROMagar ESBL CHROMagar Pseudomonas CHROMagar Strep A COLOREX Acinetobacter (MDR) COLOREX O157 CHROMagar Mastitis COLOREX mSuperCARBA COLOREX C. perfringens COLOREX B. cereus COLOREX Mastitis COLOREX Pseudomonas COLOREX Enterobacteria COLOREX Campylobacter COLOREX Y. enterocolitica CHROMagar Candida COLOREX Salmonella Plus COLOREX Serratia COLOREX Candida Plus CHROMagar CCA COLOREX COL-APSE COLOREX Staphylococcus CHROMagar STEC COLOREX Cronobacter CHROMagar mSuperCARBA CHROMagar LIN-R CHROMagar Candida Plus COLOREX Strep B COLOREX TBX CHROMagar Listeria Identification CHROMagar COL-APSE CHROMagar Malassezia CHROMagar Strep ACG COLOREX E. coli CHROMagar Staph aureus COLOREX Salmonella CHROMagar KPC COLOREX Acinetobacter CHROMagar Y. enterocolitica CHROMagar Enterobacteria CHROMagar ECC COLOREX KPC COLOREX Vibrio

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JTM Anaerobic Box Glove Microbiology Class 1 866.2120 2025-08-13
JSH Culture Media, Non-Selective And Differential Microbiology Class 1 866.2320 2024-06-20
KZJ Device, Gas Generating Microbiology Class 1 866.2580 2025-08-13
KZJ Device, Gas Generating Microbiology Class 1 866.2580 2025-08-13
JSI Culture Media, Selective And Differential Microbiology Class 1 866.2360 2025-08-13

Official Correspondent

Eva Dempsey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

K&R Technologies dba Microbiology International
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K862389 Otisville Biotech, Inc. BIOTIS ACETAMIDE AGAR 1986-07-03
K811644 Hardy Media HEKTOEN ENTERIC AGAR 1981-07-02
K832535 Otisville Biotech, Inc. HEKTOEN ENTERIC AGAR PLATE 1983-10-04
K811331 Acumedia Manufacturers, Inc. SF BROTH 1981-05-29
K872058 Orion Corp. ORICULT-N CULTURE-PADDLE 1987-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013823481. Last updated year: 2026. Please use registration number 3013823481 when referencing this establishment in official correspondence.
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