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FDA 510(k), K761179, PSORALITE
FDA 510(k), K761179, PSORALITE
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510(K) Number: K761179
Device Name: PSORALITE
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 12/02/1976
Decision Date: 05/03/1977
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PSORALITE
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 12/02/1976
Decision Date: 05/03/1977
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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