SALONMAY BUSTLINE INCREASER— 510(k) K770082

Name: FDA 510(k) clearance K770082
Creator: U.S. Food and Drug Administration
Published: 1977-03-16

Substantially Equivalent

Gamma Enterprises, Inc.

FDA 510(k) clearance K770082 for SALONMAY BUSTLINE INCREASER, Substantially Equivalent on 1977-03-16. Applicant: Gamma Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Gamma Enterprises, Inc.
Product code: Code MWZ
Device class: Class 1
Regulation: 21 CFR 890.5660
Advisory panel: Physical Medicine
Date received: 1977-01-14
Decision date: 1977-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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