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BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK

K932057 Class II Traditional
Decision Date
1994-08-05
Sponsor / Applicant
Board of Directors, Albert Browne , Ltd.

Technical Specification

510(k) Submission ID K932057
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 1994-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK received FDA 510(k) clearance under submission number K932057, sponsored by Board of Directors, Albert Browne , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1994-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.