Pdg Product Design Group Inc
FDA Regulatory Profile
Pdg Product Design Group Inc appears in FDA public data with 1 recall, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2695-2014, Class II) was initiated on June 12, 2012. Its most recent 510(k) clearance was granted on June 27, 2017.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2695-2014 | Class II | Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr | June 12, 2012 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K163432 | Stellar LEAP | June 27, 2017 |
| K140023 | ELEVATION | October 16, 2014 |
| K063736 | FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 | January 17, 2007 |
| K061475 | ASTROTILT MANUAL WHEELCHAIR | June 14, 2006 |
| K990557 | THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR | March 22, 1999 |
| K971389 | ECLIPSE 400 MANUALLY OPERATED WHEELCAIR | May 9, 1997 |
| K970311 | BENTLEY MANUALLY OPERATED WHEELCHAIR | February 14, 1997 |
| K961743 | ECLIPSE 600 MANUALLY OPERATED WHEELCHAIR | May 29, 1996 |