510(k) K912599
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 11, 1991
- Date Received
- June 10, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
- Device Class
- Class II
- Regulation Number
- 870.5550
- Review Panel
- CV
- Submission Type