PERFUSION MONITOR— 510(k) K900860
Substantially EquivalentCardio Metrics, Inc.
FDA 510(k) clearance K900860 for PERFUSION MONITOR, Substantially Equivalent on 1990-08-14. Applicant: Cardio Metrics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardio Metrics, Inc.
- Product code
- Code DTY
- Device class
- Class 2
- Regulation
- 21 CFR 870.4410
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sugar Land, TX, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.