Psoralite Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Psoralite Corp. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Psoralite Corp. has 4 FDA 510(k) cleared medical devices. Based in Columbia, US.
Historical record: 4 cleared submissions from 1987 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Psoralite Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Psoralite Corp.
5 devices
Cleared
Oct 28, 1991
PSORALITE , PHOTOTHERAPY TREATMENT EQUIPMENT
General & Plastic Surgery
67d
Cleared
May 11, 1989
PSORALITE PHOTOTHERAPY TREATMENT BOOTH, MDL 45000
General & Plastic Surgery
121d
Cleared
Apr 13, 1988
PSORALITE PHOTOTHERAPY TREATMENT BOOTH/PANEL
General & Plastic Surgery
9d
Cleared
Feb 04, 1987
PSORALITE 12800 SERIES
General & Plastic Surgery
82d
Cleared
Feb 04, 1987
PSORALITE 18400 SERIES
General & Plastic Surgery
82d