The following data is part of a premarket notification filed by Medmetric Corp. with the FDA for Torque Frame Qtf1000.
| Device ID | K904898 |
| 510k Number | K904898 |
| Device Name: | TORQUE FRAME QTF1000 |
| Classification | System, Isokinetic Testing And Evaluation |
| Applicant | MEDMETRIC CORP. 7542 TRADE ST. San Diego, CA 92121 -2412 |
| Contact | Watkins |
| Correspondent | Watkins MEDMETRIC CORP. 7542 TRADE ST. San Diego, CA 92121 -2412 |
| Product Code | IKK |
| CFR Regulation Number | 890.1925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-30 |
| Decision Date | 1990-11-28 |