The following data is part of a premarket notification filed by Optus, Inc. with the FDA for Optus Cystoscopes And Pediatric Cystoscopes.
| Device ID | K945262 |
| 510k Number | K945262 |
| Device Name: | OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPES |
| Classification | Cystoscope And Accessories, Flexible/rigid |
| Applicant | OPTUS, INC. 1200 SOUTH PARKER RD. Denver, CO 80231 |
| Contact | Peter Duffy |
| Correspondent | Peter Duffy OPTUS, INC. 1200 SOUTH PARKER RD. Denver, CO 80231 |
| Product Code | FAJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-10-28 |
| Decision Date | 1995-05-26 |