ONCE-A-DAY BOWIE AND DICK TEST PACK.— 510(k) K961156

Name: FDA 510(k) clearance K961156
Creator: U.S. Food and Drug Administration
Published: 1997-04-01

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K961156 for ONCE-A-DAY BOWIE AND DICK TEST PACK., Substantially Equivalent on 1997-04-01. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1996-03-22
Decision date: 1997-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island, NY, US

Download summary PDF View on FDA.gov ↗

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