ADAIR/VERESS NEEDLE INTRODUCER SET— 510(k) K930568

Name: FDA 510(k) clearance K930568
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

Medical Dynamics, Inc.

FDA 510(k) clearance K930568 for ADAIR/VERESS NEEDLE INTRODUCER SET, Substantially Equivalent on 1993-07-22. Applicant: Medical Dynamics, Inc.. Device class: 1.

Clearance details

Applicant: Medical Dynamics, Inc.
Product code: Code GCB
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1993-01-26
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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