Germaine Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K051727 | AIMSTICK URINE REAGENT STRIPS | October 26, 2005 |
| K013857 | AIMSTEP PREGNANCY | January 22, 2002 |
| K991369 | ACCUDIP HOME PREGNANCY AND/OR AIMSTICK PREGNANCY | May 10, 1999 |
| K981165 | AIMSTEP COMBO PREGNANCY, 1 TEST, 30 TEST, 50 TEST, 100 TEST | April 16, 1998 |
| K980531 | AIMSTEP PREGNANCY | March 6, 1998 |
| K974512 | AIMSTICK PBD COMBO PREGNANCY | January 2, 1998 |
| K974368 | AIMSTICK PBD PREGNANCY | January 2, 1998 |
| K973825 | MIDSTREAM HOME REGNANCY TEST | December 19, 1997 |