CASPAR SCALP CLIP, APPLIER— 510(k) K890443

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K890443 for CASPAR SCALP CLIP, APPLIER, Substantially Equivalent on 1989-06-15. Applicant: Aesculap Instruments Corp..

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code HBO
Advisory panel: Neurology
Date received: 1989-01-27
Decision date: 1989-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, CA, US

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