HOOK PROBE— 510(k) K854890

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K854890 for HOOK PROBE, Substantially Equivalent on 1986-05-02. Applicant: Euro-Med Intl..

Clearance details

Applicant: Euro-Med Intl.
Product code: Code KDC
Advisory panel: General, Plastic Surgery
Date received: 1985-12-06
Decision date: 1986-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

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