Latex Medical Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K896986 | BLOOD PRESSURE CUFF | March 6, 1990 |
| K820175 | O.N.A.T. | January 29, 1982 |
| K812102 | O.N.A.T. | August 31, 1981 |