PERFUSION MONITOR— 510(k) K900860

Substantially Equivalent

Cardio Metrics, Inc.

FDA 510(k) clearance K900860 for PERFUSION MONITOR, Substantially Equivalent on 1990-08-14. Applicant: Cardio Metrics, Inc..

Clearance details

Applicant: Cardio Metrics, Inc.
Product code: Code DTY
Advisory panel: Cardiovascular
Date received: 1990-02-23
Decision date: 1990-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sugar Land, TX, US

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