PHLEBOPUMP, MODEL 1000— 510(k) K003284

Substantially Equivalent

Prevent Products, Inc.

FDA 510(k) clearance K003284 for PHLEBOPUMP, MODEL 1000, Substantially Equivalent on 2001-01-17. Applicant: Prevent Products, Inc.. Device class: 2.

Clearance details

Applicant: Prevent Products, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2000-10-19
Decision date: 2001-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: W St Paul, MN, 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.