510(k) K854132
K854132 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK PACEMAKER 332T, SERIES R BIPOLAR CARDIAC PULS". The FDA issued a decision of Substantially Equivalent on December 3, 1985. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Cook Pacemaker Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 1985
- Date Received
- October 10, 1985
- 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