AWARENESS TECHNOLOGY, INC.

FDA Device Registration & Listing · PALM CITY, FL, US · Registration 1036223

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
1036223
FEI Number
1036223
Entity Name
AWARENESS TECHNOLOGY, INC.
City/State/Country
PALM CITY, FL, US
Establishment Address
1935 S.W. MARTIN HWY., PALM CITY, FL 34990, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AWARENESS TECHNOLOGY, INC. (Owner Number: 1036223)
Owner / Operator Contact Address
1935 S.W. MARTIN HWY., --, Palm City, FL 34990, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

STAT FAX 2200 CHEMWELL STAT WASH

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JTQ Bath, Incubators/Water, All Microbiology Class 1 866.2540 1992-07-07
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use Clinical Chemistry Class 1 862.2300 1992-07-07
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 1994-04-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AWARENESS TECHNOLOGY, INC.
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
K760232 Instrumentation Laboratory CO PRINTER, IL 460 1976-08-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1036223. Last updated year: 2026. Please use registration number 1036223 when referencing this establishment in official correspondence.
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