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FDA 510(k), K020227, SELICOR, MODELS A100 & D100
FDA 510(k), K020227, SELICOR, MODELS A100 & D100
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510(K) Number: K020227
Device Name: SELICOR, MODELS A100 & D100
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: 01/22/2002
Decision Date: 07/30/2002
Regulation Medical Specialty: Physical Medicine
Device Name: SELICOR, MODELS A100 & D100
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: 01/22/2002
Decision Date: 07/30/2002
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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