DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY— 510(k) K960456

Name: FDA 510(k) clearance K960456
Creator: U.S. Food and Drug Administration
Published: 1996-04-01

Substantially Equivalent

Denver Biomaterials, Inc.

FDA 510(k) clearance K960456 for DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY, Substantially Equivalent on 1996-04-01. Applicant: Denver Biomaterials, Inc.. Device class: 1.

Clearance details

Applicant: Denver Biomaterials, Inc.
Product code: Code KDD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1996-01-30
Decision date: 1996-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Evergreen, CO, US

Download summary PDF View on FDA.gov ↗

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