The following data is part of a premarket notification filed by Karl Storz Endoscopy with the FDA for Ksea C-mount Arthroscopes.
| Device ID | K983142 |
| 510k Number | K983142 |
| Device Name: | KSEA C-MOUNT ARTHROSCOPES |
| Classification | Arthroscope |
| Applicant | KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | Kevin Kennan |
| Correspondent | Kevin Kennan KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-09-08 |
| Decision Date | 1998-12-07 |
| Summary: | summary |