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Arthrocare Corp.

112 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ARTHROCARE SINUS ELECTROSURGERY SYSTEM (K973478)Arthrocare Corp.1998-01-09
ARTHROCARE ELECTROSURGERY SYSTEM (K971532)Arthrocare Corp.1997-07-23
ARTHROCARE MONOPOLAR ELECTROSURGERY LOOP (K970526)Arthrocare Corp.1997-05-28
ARTHROCARE DERMATOLOGIC ELECTROSURGERY SYSTEM (K964849)Arthrocare Corp.1997-04-14
ARTHROCARE ARTHROSCOPIC ELETROSURGERY SYSTEM (MODEL 980) (K963123)Arthrocare Corp.1996-10-08
ARTHROCARE DENTAL ELECTROSURGERY SYSTEM (K962445)Arthrocare Corp.1996-07-30
ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 (K962321)Arthrocare Corp.1996-07-19
ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) (K961747)Arthrocare Corp.1996-07-15
ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM (K961069)Arthrocare Corp.1996-05-28
ARTHROCARE BIPOLAR LOOP ELECTRODE SYSTEM (K955531)Arthrocare Corp.1996-02-21
ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODIFICATION) (K953659)Arthrocare Corp.1995-09-29
ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 (K943450)Arthrocare Corp.1995-03-13
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