Company ยท US
Jace Systems, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1994. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 22, 1994 | K933059 | ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD. Jace Systems, Inc. | BXB |
| Jun 22, 1994 | K931016 | JACE MODEL H440 HAND CPM DEVICE Jace Systems, Inc. | JFA |
| Oct 8, 1993 | K931781 | JACE TRI-STIM DEVICE Jace Systems, Inc. | IPF |
| Jun 11, 1992 | K922185 | JACE KNEE EXTENSION SYSTEM -- MODIFICATION Jace Systems, Inc. | BXB |
| May 4, 1992 | K921351 | JACE MODEL PM-410 HAND CPM DEVICE Jace Systems, Inc. | JFA |
| Feb 11, 1992 | K920380 | JACE MODEL W550 WRIST CPM DEVICE Jace Systems, Inc. | BXB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||