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FDA 510(k), K973865, BIRTCHER UV LAMP
FDA 510(k), K973865, BIRTCHER UV LAMP
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510(K) Number: K973865
Device Name: BIRTCHER UV LAMP
Manufacturer: MEDFAXX, INC.
Device Classification Name: Lamp, Uvc, (For Treating Skin And Wounds)
Regulation Number: 878.4630
Classification Product Code: MXG
Date Received: 10/06/1997
Decision Date: 02/26/1999
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BIRTCHER UV LAMP
Manufacturer: MEDFAXX, INC.
Device Classification Name: Lamp, Uvc, (For Treating Skin And Wounds)
Regulation Number: 878.4630
Classification Product Code: MXG
Date Received: 10/06/1997
Decision Date: 02/26/1999
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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