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FDA 510(k), K162240, ProMedTek Model C1400 Shortwave Diathermy Device
FDA 510(k), K162240, ProMedTek Model C1400 Shortwave Diathermy Device
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510(K) Number: K162240
Device Name: ProMedTek Model C1400 Shortwave Diathermy Device
Manufacturer: PROMEDTEK INC.
Device Classification Name: diathermy, shortwave, for use in applying therapeutic deep heat
Regulation Number: 890.5290
Classification Product Code: IMJ
Date Received: 08/09/2016
Decision Date: 11/17/2016
Regulation Medical Specialty: Physical Medicine
Device Name: ProMedTek Model C1400 Shortwave Diathermy Device
Manufacturer: PROMEDTEK INC.
Device Classification Name: diathermy, shortwave, for use in applying therapeutic deep heat
Regulation Number: 890.5290
Classification Product Code: IMJ
Date Received: 08/09/2016
Decision Date: 11/17/2016
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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