The following data is part of a premarket notification filed by Medmetric Corp. with the FDA for Kt2000 Knee Ligament Arthrometer.
| Device ID | K942059 |
| 510k Number | K942059 |
| Device Name: | KT2000 KNEE LIGAMENT ARTHROMETER |
| Classification | Arthrometer |
| Applicant | MEDMETRIC CORP. 7542 TRADE ST. San Diego, CA 92121 -2412 |
| Contact | K.r. Watkins |
| Correspondent | K.r. Watkins MEDMETRIC CORP. 7542 TRADE ST. San Diego, CA 92121 -2412 |
| Product Code | LYH |
| CFR Regulation Number | 890.1615 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-04-29 |
| Decision Date | 1994-09-20 |