ClearanceBrief
Company ยท US

Inman Liebelt Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 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
FAQBag, Urine Collection, Leg, For External Use, Sterile1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
HDAForceps, Obstetrical1
KMKDevice, Intravascular Catheter Securement1
KNYAccessories, Catheter, G-U1
OCTAnti Fog Solution And Accessories, Endoscopy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 9, 1991K912211INTRAVASCULAR CATHETER SECURMENT DEVICE
Inman Liebelt Corp.
KMK
Jul 26, 1991K912146URETERAL CATHETER HOLDER
Inman Liebelt Corp.
KNY
May 10, 1991K905590UCEZ - STERILE LENS FOG REDUCTION DEVICE
Inman Liebelt Corp.
OCT
Apr 12, 1991K905583ILC FORCEPS PADS
Inman Liebelt Corp.
HDA
Oct 26, 1990K903611ILC LEG BAG HOLDER
Inman Liebelt Corp.
FAQ
Oct 19, 1990K903610O.R. TIP CLEANER
Inman Liebelt Corp.
GEI

Latest recalls

DateFirm and productCodeLinked 510(k)
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