Kinetic Medical Products
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 63
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K890385 | MIDWIFERY/OBSTETRICAL FORCEPS | March 1, 1989 |
| K890382 | COMPRESSION FORCEPS | February 27, 1989 |
| K890387 | MALLEABLE PLACENTA CURETTE | February 27, 1989 |
| K890376 | VAGINAL SPECULUM | February 27, 1989 |
| K890380 | CERVICAL BIOPSY FORCEPS | February 27, 1989 |
| K890216 | MICROSURGICAL KERATOME | February 16, 1989 |
| K890383 | HYSTERECTOMY FORCEPS | February 16, 1989 |
| K890379 | UTERINE TENTACULUM | February 13, 1989 |
| K890388 | CEPHALOTOMY SCISSORS | February 13, 1989 |
| K890375 | VAGINAL SPECULUM | February 13, 1989 |
| K890377 | FIXED-SIZE UTERINE DILATOR | February 13, 1989 |
| K890389 | UMBILICAL SCISSORS | February 13, 1989 |
| K890378 | UTERINE DRESSING FORCEPS | February 13, 1989 |
| K890386 | PLACENTA AND OVUM FORCEPS | February 13, 1989 |
| K890384 | UTERINE CURETTE | February 13, 1989 |
| K890369 | GALL STONE FORCEPS | February 3, 1989 |
| K890373 | HEMORRHOIDAL FORCEPS | February 3, 1989 |
| K890365 | SEPTUM ELEVATOR | February 3, 1989 |
| K890366 | ADENOID CURETTE | February 3, 1989 |
| K890368 | KIDNEY CLAMP | February 3, 1989 |