The following data is part of a premarket notification filed by Medscope Corp. with the FDA for Medscope 4mm Arthroscope.
| Device ID | K894303 |
| 510k Number | K894303 |
| Device Name: | MEDSCOPE 4MM ARTHROSCOPE |
| Classification | Arthroscope |
| Applicant | MEDSCOPE CORP. 495 LINDBERG LN. Northbrook, IL 60062 |
| Contact | Joachim Spiess |
| Correspondent | Joachim Spiess MEDSCOPE CORP. 495 LINDBERG LN. Northbrook, IL 60062 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-23 |
| Decision Date | 1989-07-25 |