The following data is part of a premarket notification filed by Jace Systems, Inc. with the FDA for Artromot-e, Elbow / Artromot-s, Shoulder Cmp Mod..
| Device ID | K933059 |
| 510k Number | K933059 |
| Device Name: | ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD. |
| Classification | Exerciser, Powered |
| Applicant | JACE SYSTEMS, INC. 101 FOSTER RD. Moorestown, NJ 08057 |
| Contact | Rick Rosati |
| Correspondent | Rick Rosati JACE SYSTEMS, INC. 101 FOSTER RD. Moorestown, NJ 08057 |
| Product Code | BXB |
| CFR Regulation Number | 890.5380 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-22 |
| Decision Date | 1994-06-22 |