The following data is part of a premarket notification filed by Dyonics, Inc. with the FDA for Dynamic Cruciate Tester.
| Device ID | K881876 |
| 510k Number | K881876 |
| Device Name: | DYNAMIC CRUCIATE TESTER |
| Classification | Arthrometer |
| Applicant | DYONICS, INC. 160 DASCOMB RD. Andover, MA 01810 |
| Contact | Kenneth E Carrier |
| Correspondent | Kenneth E Carrier DYONICS, INC. 160 DASCOMB RD. Andover, MA 01810 |
| Product Code | LYH |
| CFR Regulation Number | 890.1615 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-04 |
| Decision Date | 1988-11-17 |