SKYTRON ELITE 300 SURGERY TABLE— 510(k) K853479

Name: FDA 510(k) clearance K853479
Creator: U.S. Food and Drug Administration
Published: 1985-09-05

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K853479 for SKYTRON ELITE 300 SURGERY TABLE, Substantially Equivalent on 1985-09-05. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 1.

Clearance details

Applicant: Skytron, Div. the Kmw Group, Inc.
Product code: Code FWW
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1985-08-20
Decision date: 1985-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

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