AESCULAP POWER SYSTEM HANDPIECE— 510(k) K960473

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K960473 for AESCULAP POWER SYSTEM HANDPIECE, Substantially Equivalent on 1996-03-07. Applicant: Aesculap, Inc.. Device class: 1.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code GET
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1996-02-01
Decision date: 1996-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, 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.