The following data is part of a premarket notification filed by Mednet, Inc. with the FDA for Med-net Stopcocks.
| Device ID | K955782 |
| 510k Number | K955782 |
| Device Name: | MED-NET STOPCOCKS |
| Classification | Stopcock, I.v. Set |
| Applicant | MEDNET, INC. 10572 MAHONEY DR. Sunland, CA 91040 |
| Contact | Robert T Merick |
| Correspondent | Robert T Merick MEDNET, INC. 10572 MAHONEY DR. Sunland, CA 91040 |
| Product Code | FMG |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-12-21 |
| Decision Date | 1996-02-21 |