DeviceClearance

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.. Device class: 2.

Clearance details

Applicant
Perimed, Inc.
Product code
Code DPW
Device class
Class 2
Regulation
21 CFR 870.2100
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Piscataway, NJ, US
Download summary PDFView on FDA.gov ↗

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