TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT— 510(k) K961368

Name: FDA 510(k) clearance K961368
Creator: U.S. Food and Drug Administration
Published: 1996-10-11

Unknown

Vasamedics, LLC

FDA 510(k) clearance K961368 for TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT, Unknown on 1996-10-11. Applicant: Vasamedics, LLC. Device class: 2.

Clearance details

Applicant: Vasamedics, LLC
Product code: Code DPT
Device class: Class 2
Regulation: 21 CFR 870.2120
Advisory panel: Cardiovascular
Date received: 1996-04-09
Decision date: 1996-10-11
Decision: Unknown
Clearance type: Traditional
Location: Saint Paul, MN, US

Download summary PDF View on FDA.gov ↗

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