FDA 510(k), K030382, SELITHERM, MODEL C100

510(K) Number: K030382
Device Name: SELITHERM, MODEL C100
Manufacturer: SELICOR, INC.
Device Classification Name: diathermy, shortwave, for use in applying therapeutic deep heat
Regulation Number: 890.5290
Classification Product Code: IMJ
Date Received: 02/05/2003
Decision Date: 04/01/2003
Regulation Medical Specialty: Physical Medicine

Total pages: 180
Fully redacted pages: 121
Content pages: 59