1
/
of
0
FDA 510(k), K820492, SPECTRA305
FDA 510(k), K820492, SPECTRA305
Regular price
$149.00 USD
Regular price
Sale price
$149.00 USD
Unit price
/
per
510(K) Number: K820492
Device Name: SPECTRA305
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 02/23/1982
Decision Date: 03/31/1982
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SPECTRA305
Manufacturer: ULTRALITE
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 02/23/1982
Decision Date: 03/31/1982
Regulation Medical Specialty: General & Plastic Surgery
Couldn't load pickup availability
- 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.
View full details