SENTRA— 510(k) K843060
Substantially EquivalentCardiac Pacemakers, Inc.
FDA 510(k) clearance K843060 for SENTRA, Substantially Equivalent on 1984-09-20. Applicant: Cardiac Pacemakers, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardiac Pacemakers, Inc.
- Product code
- Code DTD
- Device class
- Class 2
- Regulation
- 21 CFR 870.3620
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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