Jace Systems, Inc.
Jace Systems, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 22, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K933059 | ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD. | June 22, 1994 |
| K931016 | JACE MODEL H440 HAND CPM DEVICE | June 22, 1994 |
| K931781 | JACE TRI-STIM DEVICE | October 8, 1993 |
| K922185 | JACE KNEE EXTENSION SYSTEM -- MODIFICATION | June 11, 1992 |
| K921351 | JACE MODEL PM-410 HAND CPM DEVICE | May 4, 1992 |
| K920380 | JACE MODEL W550 WRIST CPM DEVICE | February 11, 1992 |