PERIFLUX PF3— 510(k) K890828

Substantially Equivalent

Perimed, Inc.

FDA 510(k) clearance K890828 for PERIFLUX PF3, Substantially Equivalent on 1989-06-20. Applicant: Perimed, Inc..

Clearance details

Applicant: Perimed, Inc.
Product code: Code DPW
Advisory panel: Cardiovascular
Date received: 1989-02-21
Decision date: 1989-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Piscataway, NJ, US

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