CARDIOTEST 2200— 510(k) K790503
Substantially EquivalentCardiac Pacemakers, Inc.
FDA 510(k) clearance K790503 for CARDIOTEST 2200, Substantially Equivalent on 1979-05-17. Applicant: Cardiac Pacemakers, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardiac Pacemakers, Inc.
- Product code
- Code DTA
- Device class
- Class 2
- Regulation
- 21 CFR 870.3720
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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