CIVCO PROBE BOOT/CORD COVER— 510(k) K943393

Name: FDA 510(k) clearance K943393
Creator: U.S. Food and Drug Administration
Published: 1995-02-02

Substantially Equivalent

CIVCO Medical Instruments Co., Inc.

FDA 510(k) clearance K943393 for CIVCO PROBE BOOT/CORD COVER, Substantially Equivalent on 1995-02-02. Applicant: CIVCO Medical Instruments Co., Inc.. Device class: 2.

Clearance details

Applicant: CIVCO Medical Instruments Co., Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1994-07-14
Decision date: 1995-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalona, IA, US

Download summary PDF View on FDA.gov ↗

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