ClearanceBrief
Company ยท US

Stiefel Research Institute, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1992. 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
GEHUnit, Cryosurgical, Accessories2
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1
KOMAdhesive, Denture, Acacia And Karaya With Sodium Borate1
KOTCarboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium1
NADDressing, Wound, Occlusive1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 14, 1992K914591L.C.S. 2000 SYSTEM
Stiefel Research Institute, Inc.
GEH
Mar 29, 1991K910216STEADFAST DENTURE ADHESIVE POWDER
Stiefel Research Institute, Inc.
KOM
Apr 3, 1990K895818STEADFAST DENTURE ADHESIVE CREAM
Stiefel Research Institute, Inc.
KOT
Jan 19, 1990K895817HERMAL WOUND CARE KIT
Stiefel Research Institute, Inc.
NAD
Jan 9, 1990K896724CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.
Stiefel Research Institute, Inc.
GEH
Sep 21, 1989K893996CUSIS ULTRASOUND SKIN IMAGING SYSTEM
Stiefel Research Institute, Inc.
IYO

Latest recalls

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