510(k) K022475
- Device
- MODIFICATION TO ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000), ARTHROCARE PATIENT CABLE, FOOT CONTROL, POWER CORD, WANDS
- Applicant
- Arthrocare Corp.
- 510(k) number
- K022475
- Product code
- GEI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2002-10-03
- Date received
- 2002-07-29
- Regulation
- 878.4400
- Classification name
- Electrosurgical, Cutting & Coagulation & Accessories
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- N
Applicant Contact#
- Contact
- VALERIE DEFIESTA-NG
- Address
- 680 Vaqueros Ave. Sunnyvale CA US 94085 94085
FDA Registration Numbers#
- 1123137
- 3016746323
- 2954783
- 3006451981
- 2245304
- 2150060
- 3003678543
- 3004215117
- 3004105270
- 8010047
- 3010511300
- 1060680
- 3040993693
- 3013500228
- 3032391
- 3008215723
- 3009903460
- 3005562917
- 3005064943
- 3010041511
- 1923569
- 3008791915
- 3010687973
- 3005350457
- 3012460907
- 3010432890
- 3008729892
- 3010131466
- 3006990600
- 9616696
- 9613793
- 3013563737
- 3020623326
- 3010131137
- 3009420598
- 3015173212
- 3005083075
- 3015453963
- 1724474
- 3004519921
- 3033589330
- 1313525
- 3027339877
- 2183319
- 3013734919
- 3008720584
- 3014939461
- 3004636440
- 3012497308
- 3031916226
- 3016087306
- 9614279
- 3027988352
- 9680001
- 3002858762
- 3015241782
- 3008816935
- 3013111980
- 2030598
- 1418975
- 3002807090
- 2183785
- 3007710878
- 9680515
- 3015460875
- 3017202975
- 9680952
- 9611612
- 3016248634
- 3001675293
- 3009166798
- 3043532708
- 3038988287
- 2529846
- 3007791595
- 3003755939
- 1820334
- 1219930
- 3008849319
Source Documents#
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