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FDA 510(k), K827123, SPECTRA (ULTRAVIOLET PRODUCTS)
FDA 510(k), K827123, SPECTRA (ULTRAVIOLET PRODUCTS)
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510(K) Number: K827123
Device Name: SPECTRA (ULTRAVIOLET PRODUCTS)
Manufacturer: ULTRALITE
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 02/02/1982
Decision Date: 03/05/1982
Regulation Medical Specialty:
Device Name: SPECTRA (ULTRAVIOLET PRODUCTS)
Manufacturer: ULTRALITE
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 02/02/1982
Decision Date: 03/05/1982
Regulation Medical Specialty:
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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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