MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A— 510(k) K875179

Name: FDA 510(k) clearance K875179
Creator: U.S. Food and Drug Administration
Published: 1988-09-19

Substantially Equivalent

Tsi, Inc.

FDA 510(k) clearance K875179 for MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A, Substantially Equivalent on 1988-09-19. 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: 1987-12-17
Decision date: 1988-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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