MOSSMAN ASSOCIATES, INC.

FDA Device Registration & Listing · Milford, MA, US · Registration 3002622685

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
3002622685
FEI Number
3002622685
Entity Name
MOSSMAN ASSOCIATES, INC.
City/State/Country
Milford, MA, US
Establishment Address
9 Village Circle, Milford, MA 01757, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Mossman Associates, Inc. (Owner Number: 10024170)
Owner / Operator Contact Address
9 Village Circle, Milford, MA 01757, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K963733
PMA Number
N/A

All Registered Proprietary Names

NicCheck Instant Nicotine Detection Test for Nicotine and Its Metabol

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRS Test System, Nicotine, Cotinine, Metabolites Clinical Toxicology Class 1 862.3220 2008-01-08
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2008-01-08

Official Correspondent

Donald Mossman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mossman Associates, 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 3002622685. Last updated year: 2026. Please use registration number 3002622685 when referencing this establishment in official correspondence.
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