PERIFLUX PF4001 LASER DOPPLER FLOWMETER— 510(k) K922368

Substantially Equivalent

Perimed, Inc.

FDA 510(k) clearance K922368 for PERIFLUX PF4001 LASER DOPPLER FLOWMETER, Substantially Equivalent on 1993-02-03. Applicant: Perimed, Inc..

Clearance details

Applicant: Perimed, Inc.
Product code: Code DPW
Advisory panel: Cardiovascular
Date received: 1992-05-20
Decision date: 1993-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Piscataway, NJ, US

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