ClearanceBrief
Company ยท US

Gil-Med Industries C/O Kegan & Kegan, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1988. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KPEContainer, I.V.4
KNTTubes, Gastrointestinal (And Accessories)2
KNXCollector, Urine, (And Accessories) For Indwelling Catheter1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 20, 1988K880506MODIFIED EVA-MIX AND DI-MIX BAGS
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KPE
Feb 10, 1987K870274DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KPE
Aug 11, 1986K861862DIETO CONTAINER FOR ENTERAL NUTRITION
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KNT
Oct 26, 1984K841597GIL-MED PARENTERAL NUTRITION OR MEDICINE
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KPE
May 2, 1984K841224URO-MALE INCONTINENCE CATHETER
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KNX
Apr 17, 1984K840915DIMIX CONTAINER FOR PARNETERAL NUTRIT
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KPE
Apr 4, 1984K840916DIETO CONTAINER FOR ENTERNAL NUTRIT
Gil-Med Industries C/O Kegan & Kegan, Ltd.
KNT

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes