FDA 510(k), K082819, DERMATOLOGIC TREATMENT SYSTEM (DTS) G2

FDA 510(k), K082819, DERMATOLOGIC TREATMENT SYSTEM (DTS) G2

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510(K) Number: K082819
Device Name: DERMATOLOGIC TREATMENT SYSTEM (DTS) G2
Manufacturer:
Device Classification Name: System, Ablation, Microwave And Accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 09/25/2008
Decision Date: 03/20/2009
Regulation Medical Specialty: General & Plastic Surgery
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