EXPANDACELL INSTRUMENT WIPE— 510(k) K960621

Name: FDA 510(k) clearance K960621
Creator: U.S. Food and Drug Administration
Published: 1996-04-01

Substantially Equivalent

Shippert Medical Technologies Corp.

FDA 510(k) clearance K960621 for EXPANDACELL INSTRUMENT WIPE, Substantially Equivalent on 1996-04-01. Applicant: Shippert Medical Technologies Corp.. Device class: 1.

Clearance details

Applicant: Shippert Medical Technologies Corp.
Product code: Code GEC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1996-02-13
Decision date: 1996-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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