MICRO-CRAFT OSCILLATING SAW HANDPIECE— 510(k) K822790

Name: FDA 510(k) clearance K822790
Creator: U.S. Food and Drug Administration
Published: 1982-10-22

Substantially Equivalent

Xomed, Inc.

FDA 510(k) clearance K822790 for MICRO-CRAFT OSCILLATING SAW HANDPIECE, Substantially Equivalent on 1982-10-22. Applicant: Xomed, Inc.. Device class: 1.

Clearance details

Applicant: Xomed, Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1982-09-15
Decision date: 1982-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arnold, MO, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.