MICRO DIRECT, INC.

FDA Device Registration & Listing · LEWISTON, ME, US · Registration 1223858

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
1223858
FEI Number
1000305581
Entity Name
MICRO DIRECT, INC.
City/State/Country
LEWISTON, ME, US
Establishment Address
803 WEBSTER ST, LEWISTON, ME 04240, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
MICRO DIRECT, INC. (Owner Number: 9007705)
Owner / Operator Contact Address
840 POWNAL RD., --, Auburn, ME 04210, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K171129
PMA Number
N/A

All Registered Proprietary Names

CO Screen CO Check Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2018-03-06
JKT Gas Chromatograph, Carbon-Monoxide Clinical Toxicology Class 1 862.3220 2018-03-06

Official Correspondent

DAVID STASZAK

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MICRO DIRECT, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1223858. Last updated year: 2026. Please use registration number 1223858 when referencing this establishment in official correspondence.
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