510(k) K953417
K953417 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS". The FDA issued a decision of ST on September 29, 1995. 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
- ST ()
- Decision Date
- September 29, 1995
- Date Received
- June 8, 1995
- 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