LASERFLO BLOOD PERFUSION MONITOR 403— 510(k) K851057

Substantially Equivalent

Tsi, Inc.

FDA 510(k) clearance K851057 for LASERFLO BLOOD PERFUSION MONITOR 403, Substantially Equivalent on 1985-06-24. 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: 1985-03-14
Decision date: 1985-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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More clearances from Tsi, Inc.

K896515 — LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM21990-02-13
K875179 — MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A1988-09-19
K864259 — MODIFIED LASERFLO BLOOD PERFUSION MONITOR1987-02-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.