Arthrocare Corp.
Arthrocare Corp. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2016.
Clearances by Arthrocare Corp. — page 2
101–112 of 112- K973478 — ARTHROCARE SINUS ELECTROSURGERY SYSTEM
- K971532 — ARTHROCARE ELECTROSURGERY SYSTEM
- K970526 — ARTHROCARE MONOPOLAR ELECTROSURGERY LOOP
- K964849 — ARTHROCARE DERMATOLOGIC ELECTROSURGERY SYSTEM
- K963123 — ARTHROCARE ARTHROSCOPIC ELETROSURGERY SYSTEM (MODEL 980)
- K962445 — ARTHROCARE DENTAL ELECTROSURGERY SYSTEM
- K962321 — ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
- K961747 — ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)
- K961069 — ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM
- K955531 — ARTHROCARE BIPOLAR LOOP ELECTRODE SYSTEM
- K953659 — ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODIFICATION)
- K943450 — ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
Data sourced from openFDA. This site is unofficial and independent of the FDA.