FLOSCOPE MICRODOP— 510(k) K910441

Substantially Equivalent

Advance Medical Device, Inc.

FDA 510(k) clearance K910441 for FLOSCOPE MICRODOP, Substantially Equivalent on 1991-03-21. Applicant: Advance Medical Device, Inc..

Clearance details

Applicant: Advance Medical Device, Inc.
Product code: Code DPT
Advisory panel: Cardiovascular
Date received: 1991-01-31
Decision date: 1991-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berlin, NJ, US

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