LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2— 510(k) K896515

Name: FDA 510(k) clearance K896515
Creator: U.S. Food and Drug Administration
Published: 1990-02-13

Substantially Equivalent

Tsi, Inc.

FDA 510(k) clearance K896515 for LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2, Substantially Equivalent on 1990-02-13. Applicant: Tsi, Inc.. Device class: 2.

Clearance details

Applicant: Tsi, Inc.
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1989-11-15
Decision date: 1990-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Findley, MN, US

Download summary PDF View on FDA.gov ↗

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