Germaine Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Germaine Laboratories, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Germaine Laboratories, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 8 cleared submissions from 1997 to 2005. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Germaine Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Germaine Laboratories, Inc.
8 devices
Cleared
Oct 26, 2005
AIMSTICK URINE REAGENT STRIPS
Chemistry
120d
Cleared
Jan 22, 2002
AIMSTEP PREGNANCY
Chemistry
62d
Cleared
May 10, 1999
ACCUDIP HOME PREGNANCY AND/OR AIMSTICK PREGNANCY
Chemistry
20d
Cleared
Apr 16, 1998
AIMSTEP COMBO PREGNANCY, 1 TEST, 30 TEST, 50 TEST, 100 TEST
Chemistry
16d
Cleared
Mar 06, 1998
AIMSTEP PREGNANCY
Chemistry
23d
Cleared
Jan 02, 1998
AIMSTICK PBD PREGNANCY
Chemistry
43d
Cleared
Jan 02, 1998
AIMSTICK PBD COMBO PREGNANCY
Chemistry
32d
Cleared
Dec 19, 1997
MIDSTREAM HOME REGNANCY TEST
Chemistry
73d