The following data is part of a premarket notification filed by Surgical Technologies, Inc. with the FDA for Arthroscope.
| Device ID | K942029 |
| 510k Number | K942029 |
| Device Name: | ARTHROSCOPE |
| Classification | Arthroscope |
| Applicant | SURGICAL TECHNOLOGIES, INC. 4715 N.W. 157TH. STREET, SUITE 124 Miami Lakes, FL 33014 |
| Contact | Laszlo Fazekas |
| Correspondent | Laszlo Fazekas SURGICAL TECHNOLOGIES, INC. 4715 N.W. 157TH. STREET, SUITE 124 Miami Lakes, FL 33014 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-04-26 |
| Decision Date | 1995-11-08 |