Pacesetter, Inc.
Pacesetter, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1998.
Top product codes for Pacesetter, Inc.
Recent clearances by Pacesetter, Inc.
- K972814 — LOCATOR MODEL 4036
- K960854 — SIEMENS SERVO ULTRA NEBULIZER 345
- K954714 — AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION)
- K954551 — DF-1 TERMINAL CAP
- K951950 — PASSIVE PLUS PACING LEADS WITH TITANIUM NITRIDE COATING
- K952206 — PASSIVE PLUS PACING LEADS WITH TITANIUM NITRIDE COATING
- K951087 — TENDRIL, UNIPOLAR ENDOCARDIAL SCREW-IN LEAD
- K950140 — IS-1/QUADRIPOLAR TERMINAL CAP, PART NUMBER 6011069
Data sourced from openFDA. This site is unofficial and independent of the FDA.