ClearanceBrief
Company ยท US

Psoralite Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1991. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FTCLight, Ultraviolet, Dermatological5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 28, 1991K913760PSORALITE , PHOTOTHERAPY TREATMENT EQUIPMENT
Psoralite Corp.
FTC
May 11, 1989K890084PSORALITE PHOTOTHERAPY TREATMENT BOOTH, MDL 45000
Psoralite Corp.
FTC
Apr 13, 1988K881385PSORALITE PHOTOTHERAPY TREATMENT BOOTH/PANEL
Psoralite Corp.
FTC
Feb 4, 1987K864511PSORALITE 18400 SERIES
Psoralite Corp.
FTC
Feb 4, 1987K864510PSORALITE 12800 SERIES
Psoralite Corp.
FTC

Latest recalls

DateFirm and productCodeLinked 510(k)
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