The following data is part of a premarket notification filed by M.s. Jahanger, Md with the FDA for Dr. Jahanger's Cutter.
| Device ID | K990738 |
| 510k Number | K990738 |
| Device Name: | DR. JAHANGER'S CUTTER |
| Classification | Instrument, Manual, Specialized Obstetric-gynecologic |
| Applicant | M.S. JAHANGER, MD 440 EGG HARBOR RD. Tuenersville, NJ 08012 |
| Contact | Mohammed Jahanger |
| Correspondent | Mohammed Jahanger M.S. JAHANGER, MD 440 EGG HARBOR RD. Tuenersville, NJ 08012 |
| Product Code | KNA |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-05 |
| Decision Date | 1999-10-29 |