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FDA 510(k), K861963, ULTRALITE HF1236 HAND AND FOOT SYSTEM
FDA 510(k), K861963, ULTRALITE HF1236 HAND AND FOOT SYSTEM
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510(K) Number: K861963
Device Name: ULTRALITE HF1236 HAND AND FOOT SYSTEM
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 05/20/1986
Decision Date: 06/25/1986
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ULTRALITE HF1236 HAND AND FOOT SYSTEM
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 05/20/1986
Decision Date: 06/25/1986
Regulation Medical Specialty: General & Plastic Surgery
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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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