FORCEPS, BIOPSY(NON RIGID)— 510(k) K852120

Name: FDA 510(k) clearance K852120
Creator: U.S. Food and Drug Administration
Published: 1985-07-02

Substantially Equivalent

Scholten Surgical Instruments, Inc.

FDA 510(k) clearance K852120 for FORCEPS, BIOPSY(NON RIGID), Substantially Equivalent on 1985-07-02. Applicant: Scholten Surgical Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Scholten Surgical Instruments, Inc.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-05-15
Decision date: 1985-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redwood City, CA, US

Download summary PDF View on FDA.gov ↗

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