The following data is part of a premarket notification filed by Dyna-med with the FDA for Amx-110, Amx-ii And Amx-iii.
| Device ID | K884340 |
| 510k Number | K884340 |
| Device Name: | AMX-110, AMX-II AND AMX-III |
| Classification | Accessories, Traction |
| Applicant | DYNA-MED 3706-B E. RIO GRANDE Victoria, TX 77901 |
| Contact | Thomas, Jr |
| Correspondent | Thomas, Jr DYNA-MED 3706-B E. RIO GRANDE Victoria, TX 77901 |
| Product Code | ILZ |
| CFR Regulation Number | 890.5925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-14 |
| Decision Date | 1989-01-24 |