Reliance Medical Products Inc
FDA Regulatory Profile
Reliance Medical Products Inc appears in FDA public data with 1 recall, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1318-2018, Class II) was initiated on December 6, 2017. Its most recent 510(k) clearance was granted on September 12, 1989.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1318-2018 | Class II | Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical dev | December 6, 2017 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K894018 | RELIANCE(R) 6200 EXAMINATION CHAIR | September 12, 1989 |