Generic Medical Device, Inc.
Generic Medical Device, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 30, 2011.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K111219 | GMD UNIVERSAL URINARY INCONTINENCE SLING | June 30, 2011 |
| K083471 | GMD UNIVERSAL SLING, MODEL PRODUCT CODE 1010 AND 1020 | March 3, 2009 |
| K070018 | UNIVERSAL SURGICAL MESH, MODEL 100 | April 27, 2007 |
| K063429 | GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 | January 17, 2007 |