510(k) K760670
K760670 is an FDA 510(k) premarket notification submitted by Vitatron Medical BV for the device "PACEMAKERS, VITATRONS (SERIES 2000)". The FDA issued a decision of Substantially Equivalent on November 12, 1976. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Vitatron Medical BV has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 12, 1976
- Date Received
- September 17, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implantable Pacemaker Pulse-Generator
- Device Class
- Class III
- Regulation Number
- 870.3610
- Review Panel
- CV
- Submission Type