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BIOSTREP A, BIOSIGN STREP A, STATUSFIRST STREP A

K082661 Class I Special
Decision Date
2008-10-06
Sponsor / Applicant
Princeton BioMeditech Corp.

Technical Specification

510(k) Submission ID K082661
Product Code GTY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3740
Decision Date 2008-10-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSTREP A, BIOSIGN STREP A, STATUSFIRST STREP A received FDA 510(k) clearance under submission number K082661, sponsored by Princeton BioMeditech Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2008-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code GTY and 21 CFR 866.3740, within the Microbiology review panel as a Class I device.