The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Cleartrac Cannula.
| Device ID | K920454 |
| 510k Number | K920454 |
| Device Name: | CLEARTRAC CANNULA |
| Classification | Arthroscope |
| Applicant | ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
| Contact | Jeffrey Henderson |
| Correspondent | Jeffrey Henderson ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-04 |
| Decision Date | 1992-09-16 |