COX DISPOSABLE RETRIEVAL DEVICES— 510(k) K923489

Name: FDA 510(k) clearance K923489
Creator: U.S. Food and Drug Administration
Published: 1992-09-23

Substantially Equivalent

Cox Medical Ent., Inc.

FDA 510(k) clearance K923489 for COX DISPOSABLE RETRIEVAL DEVICES, Substantially Equivalent on 1992-09-23. Applicant: Cox Medical Ent., Inc.. Device class: 2.

Clearance details

Applicant: Cox Medical Ent., Inc.
Product code: Code OCZ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1992-07-15
Decision date: 1992-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, CA, US

Download summary PDF View on FDA.gov ↗

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