KMI OXY-BAN— 510(k) K883848

Name: FDA 510(k) clearance K883848
Creator: U.S. Food and Drug Administration
Published: 1989-03-02

Substantially Equivalent for Some Indications

Knight Medical, Inc.

FDA 510(k) clearance K883848 for KMI OXY-BAN, Substantially Equivalent for Some Indications on 1989-03-02. Applicant: Knight Medical, Inc.. Device class: 2.

Clearance details

Applicant: Knight Medical, Inc.
Product code: Code KPJ
Device class: Class 2
Regulation: 21 CFR 878.5650
Advisory panel: General, Plastic Surgery
Date received: 1988-09-12
Decision date: 1989-03-02
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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