SKYTRON ELITE SURGICAL TABLES— 510(k) K811311

Name: FDA 510(k) clearance K811311
Creator: U.S. Food and Drug Administration
Published: 1981-06-02

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K811311 for SKYTRON ELITE SURGICAL TABLES, Substantially Equivalent on 1981-06-02. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 2.

Clearance details

Applicant: Skytron, Div. the Kmw Group, Inc.
Product code: Code GBC
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1981-05-11
Decision date: 1981-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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