HOLLISTER PREMIUM URINE COLLECTOR— 510(k) K931277

Name: FDA 510(k) clearance K931277
Creator: U.S. Food and Drug Administration
Published: 1993-06-23

Substantially Equivalent

Hollister, Inc.

FDA 510(k) clearance K931277 for HOLLISTER PREMIUM URINE COLLECTOR, Substantially Equivalent on 1993-06-23. Applicant: Hollister, Inc.. Device class: 1.

Clearance details

Applicant: Hollister, Inc.
Product code: Code EXI
Device class: Class 1
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1993-03-08
Decision date: 1993-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Libertyville, IL, US

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