Pacesetter, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972814 | LOCATOR MODEL 4036 | DTB | 1998-02-23 | View |
| 510(k) | K960854 | SIEMENS SERVO ULTRA NEBULIZER 345 | CAF | 1996-12-23 | View |
| 510(k) | K954714 | AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION) | DTB | 1996-02-01 | View |
| 510(k) | K954551 | DF-1 TERMINAL CAP | DTB | 1995-12-26 | View |
| 510(k) | K952206 | PASSIVE PLUS PACING LEADS WITH TITANIUM NITRIDE COATING | DTB | 1995-08-31 | View |
| 510(k) | K951950 | PASSIVE PLUS PACING LEADS WITH TITANIUM NITRIDE COATING | DTB | 1995-08-31 | View |
| 510(k) | K951087 | TENDRIL, UNIPOLAR ENDOCARDIAL SCREW-IN LEAD | DTB | 1995-06-29 | View |
| 510(k) | K950140 | IS-1/QUADRIPOLAR TERMINAL CAP, PART NUMBER 6011069 | DTD | 1995-04-06 | View |
No matching devices.
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