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FDA 510(k), K820280, SPECTRA 305/350
FDA 510(k), K820280, SPECTRA 305/350
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$149.00 USD
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510(K) Number: K820280
Device Name: SPECTRA 305/350
Manufacturer: ULTRALITE
Device Classification Name: cabinet, phototherapy (puva)
Regulation Number: 878.4630
Classification Product Code: KGL
Date Received: 02/02/1982
Decision Date: 03/05/1982
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SPECTRA 305/350
Manufacturer: ULTRALITE
Device Classification Name: cabinet, phototherapy (puva)
Regulation Number: 878.4630
Classification Product Code: KGL
Date Received: 02/02/1982
Decision Date: 03/05/1982
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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