ClearanceBrief
Company ยท US

Rand Scientific Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1996. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HQDLens, Contact (Other Material) - Daily2
MIBElastomer, Silicone Block2
EMXBalloon, Epistaxis1
FWPProsthesis, Chin, Internal1
FZEProsthesis, Nose, Internal1
HPXLens, Contact (Polymethylmethacrylate)1
LZKImplant, Malar1
MICImplant, Muscle, Pectoralis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 18, 1996K963856RAND NASAL PACKING
Rand Scientific Corp.
EMX
May 22, 1996K961081SPIRIT RIDGE SILICONE CARVING BLOCK
Rand Scientific Corp.
MIB
May 16, 1996K961057DURALASTIC SHEETING II
Rand Scientific Corp.
MIB
May 16, 1996K955777PMMA CLASIC
Rand Scientific Corp.
HPX
Apr 19, 1996K961124THE NAUTILUS
Rand Scientific Corp.
FZE
Apr 19, 1996K961080MEDIAL MALAR IMPLANT
Rand Scientific Corp.
LZK
Apr 19, 1996K961072PEC IMPLANT
Rand Scientific Corp.
MIC
Apr 19, 1996K961071THE MAGNUM CHIN IMPLANT
Rand Scientific Corp.
FWP
Mar 28, 1996K955366TRANS-AIRE RIGID GAS PERMABLE CONTACT LENS
Rand Scientific Corp.
HQD
Jun 30, 1995K952165TRANS-AIRE RIGID GAS PERMEABLE CONTACT LENS
Rand Scientific Corp.
HQD

Latest recalls

DateFirm and productCodeLinked 510(k)
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