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

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

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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
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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