SONI-LOK SCOPE STABILIZER— 510(k) K850122

Name: FDA 510(k) clearance K850122
Creator: U.S. Food and Drug Administration
Published: 1985-02-21

Substantially Equivalent

Med Surg Designs, Inc.

FDA 510(k) clearance K850122 for SONI-LOK SCOPE STABILIZER, Substantially Equivalent on 1985-02-21. Applicant: Med Surg Designs, Inc.. Device class: 1.

Clearance details

Applicant: Med Surg Designs, Inc.
Product code: Code FXR
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1985-01-14
Decision date: 1985-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chardon, OH, US

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