FORCEPS— 510(k) K953962

Substantially Equivalent

Biopsys Medical, Inc.

FDA 510(k) clearance K953962 for FORCEPS, Substantially Equivalent on 1995-09-08. Applicant: Biopsys Medical, Inc.. Device class: 1.

Clearance details

Applicant: Biopsys Medical, Inc.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1995-08-22
Decision date: 1995-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Juan Capistrano, CA, US

Download summary PDF View on FDA.gov ↗

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