Geneva Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Geneva Laboratories, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Geneva Laboratories, Inc. has 13 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 13 cleared submissions from 1981 to 1988.
Browse the FDA 510(k) cleared devices submitted by Geneva Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Geneva Laboratories, Inc.
13 devices
Cleared
Jul 29, 1988
GENT-L-KARE STERILE URINARY LEG BAG
Gastroenterology & Urology
129d
Cleared
Jul 28, 1988
GENT-L-KARE STERILE URINARY DRAINAGE BAG CENTER
Gastroenterology & Urology
129d
Cleared
Jul 28, 1988
GENT-L-KARE CLEANSING ENEMA SET
Gastroenterology & Urology
128d
Cleared
Jun 07, 1988
GENT-L-KARE VAGINAL IRRIGATION SET
Obstetrics & Gynecology
77d
Cleared
May 02, 1986
ACCUPAC CUSTOM PACK KERLIX SQUARES
General & Plastic Surgery
24d
Cleared
Apr 15, 1986
ACCUPAC CUSTOM SKIN SCRUB KIT
General & Plastic Surgery
14d
Cleared
Aug 26, 1985
ACCUPAC CUSTOM OPERATING ROOM PROCEDURE-DK876543
General & Plastic Surgery
21d
Cleared
May 24, 1985
COOK COUNTY HOSPITAL DRESSING CHANGE SET
General & Plastic Surgery
282d
Cleared
Dec 19, 1984
GENT-L-KARE STERILE I.V. START KIT
General Hospital
47d
Cleared
Dec 04, 1984
UNIVERSITY OF CHICAGO VASCULAR ANGIOGRAM
General Hospital
120d
Cleared
Apr 27, 1983
GENT-L-SPEC DISPOS. VAGINAL SPECULUM
Obstetrics & Gynecology
50d
Cleared
Mar 09, 1983
SURE-COUNT DISPOSABLE NEEDLE COUNTER
General Hospital
181d
Cleared
Jan 15, 1981
SUPER-SPIKE TRANSFER SET
Hematology
57d