The following data is part of a premarket notification filed by Artiberia with the FDA for 9-190,9-200,9-210,9-220 Amputation Knives, Various.
| Device ID | K851752 |
| 510k Number | K851752 |
| Device Name: | 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS |
| Classification | Knife, Amputation |
| Applicant | ARTIBERIA 4518 LOS RANCHITOS San Antonio, TX 78233 |
| Contact | Gil M Sanchez |
| Correspondent | Gil M Sanchez ARTIBERIA 4518 LOS RANCHITOS San Antonio, TX 78233 |
| Product Code | GDN |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-04-25 |
| Decision Date | 1985-06-20 |