FDA 510(k) Applications for Medical Device Product Code "KOH"
(Instrument, Manual, General Obstetric-Gynecologic)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K000212 | KARL STORZ ENDOSCOPY-AMERICA, INC. | KSEA CHARDONNES MORCELLATION KNIFE | 04/21/2000 |
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