Daavlin Co. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Daavlin Co. has 5 FDA 510(k) cleared medical devices. Based in Bryan, US.
Historical record: 5 cleared submissions from 1982 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Daavlin Co. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jan 17, 2007
3 SERIES PHOTOTHERAPY CABINET
General & Plastic Surgery
43d
Cleared
Aug 26, 1993
PSORALITE
General & Plastic Surgery
189d
Cleared
Nov 25, 1985
SPECTRA 724
General & Plastic Surgery
13d
Cleared
Jan 03, 1983
UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305
Radiology
48d
Cleared
Oct 05, 1982
SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE
Radiology
15d