ClearanceBrief
Company ยท US

Ultralite

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1991. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FTCLight, Ultraviolet, Dermatological3
IOBLamp, Infrared, Non Heating1
KGLCabinet, Phototherapy (Puva)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 30, 1991K910091ULTRALITE PANELITE
Ultralite
IOB
Jun 25, 1986K861963ULTRALITE HF1236 HAND AND FOOT SYSTEM
Ultralite
FTC
Mar 31, 1982K820492SPECTRA305
Ultralite
FTC
Mar 5, 1982K827123SPECTRA (ULTRAVIOLET PRODUCTS)
Ultralite
Mar 5, 1982K820280SPECTRA 305/350
Ultralite
KGL
May 3, 1977K761179PSORALITE
Ultralite
FTC

Latest recalls

DateFirm and productCodeLinked 510(k)
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