MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES— 510(k) K882383

Name: FDA 510(k) clearance K882383
Creator: U.S. Food and Drug Administration
Published: 1988-11-28

Substantially Equivalent

CIVCO Medical Instruments Co., Inc.

FDA 510(k) clearance K882383 for MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES, Substantially Equivalent on 1988-11-28. Applicant: CIVCO Medical Instruments Co., Inc.. Device class: 2.

Clearance details

Applicant: CIVCO Medical Instruments Co., Inc.
Product code: Code DWZ
Device class: Class 2
Regulation: 21 CFR 870.4075
Advisory panel: Cardiovascular
Date received: 1988-06-09
Decision date: 1988-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalona, IA, US

Download summary PDF View on FDA.gov ↗

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