RNG SERIES ULTRASOUND NEEDLE/CATH. GDS— 510(k) K820269

Name: FDA 510(k) clearance K820269
Creator: U.S. Food and Drug Administration
Published: 1982-03-23

Substantially Equivalent

CIVCO Medical Instruments Co., Inc.

FDA 510(k) clearance K820269 for RNG SERIES ULTRASOUND NEEDLE/CATH. GDS, Substantially Equivalent on 1982-03-23. Applicant: CIVCO Medical Instruments Co., Inc.. Device class: 1.

Clearance details

Applicant: CIVCO Medical Instruments Co., Inc.
Product code: Code DWO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1982-02-02
Decision date: 1982-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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