PERIFLUX PF-2— 510(k) K844631

Substantially Equivalent

Medex, Inc.

FDA 510(k) clearance K844631 for PERIFLUX PF-2, Substantially Equivalent on 1985-02-20. Applicant: Medex, Inc.. Device class: 2.

Clearance details

Applicant: Medex, Inc.
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1984-11-27
Decision date: 1985-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hilliard, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.