The following data is part of a premarket notification filed by Karl Storz Endoscopy with the FDA for Ksea Uretero-reno-fiberscope And Nephro-fiberscope.
| Device ID | K970427 |
| 510k Number | K970427 |
| Device Name: | KSEA URETERO-RENO-FIBERSCOPE AND NEPHRO-FIBERSCOPE |
| Classification | Ureteroscope And Accessories, Flexible/rigid |
| Applicant | KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | Kevin A Kennan |
| Correspondent | Kevin A Kennan KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Product Code | FGB |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-02-04 |
| Decision Date | 1997-03-11 |
| Summary: | summary |