CARDIOPULMONARY BYPASS LEVEL SENSING MONITOR— 510(k) K910599

Name: FDA 510(k) clearance K910599
Creator: U.S. Food and Drug Administration
Published: 1993-05-20

Substantially Equivalent

Jtl Medical Corp.

FDA 510(k) clearance K910599 for CARDIOPULMONARY BYPASS LEVEL SENSING MONITOR, Substantially Equivalent on 1993-05-20. Applicant: Jtl Medical Corp.. Device class: 2.

Clearance details

Applicant: Jtl Medical Corp.
Product code: Code DTW
Device class: Class 2
Regulation: 21 CFR 870.4340
Advisory panel: Cardiovascular
Date received: 1991-02-13
Decision date: 1993-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riverside, CA, 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.