FDA 510(k) Applications for Medical Device Product Code "HNY"
(Cystotome)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K961524 | STERILAB, INC. | STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS | 05/16/1996 |
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