The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Acufex Video System.
| Device ID | K940241 |
| 510k Number | K940241 |
| Device Name: | ACUFEX VIDEO SYSTEM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
| Contact | Frederick Tobia |
| Correspondent | Frederick Tobia ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-01-19 |
| Decision Date | 1994-04-12 |