MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM2— 510(k) K912446

Name: FDA 510(k) clearance K912446
Creator: U.S. Food and Drug Administration
Published: 1991-12-12

Substantially Equivalent

Vasamedics, LLC

FDA 510(k) clearance K912446 for MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM2, Substantially Equivalent on 1991-12-12. Applicant: Vasamedics, LLC. Device class: 2.

Clearance details

Applicant: Vasamedics, LLC
Product code: Product code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1991-06-03
Decision date: 1991-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, 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.