Med USA
FDA Regulatory Profile
Med USA appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 14, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K896766 | TD-28 DISPOSABLE ELECTRODE | March 14, 1990 |
| K862047 | COAGULATOR (8 CHANNEL) | September 29, 1986 |
| K852492 | COAGULATOR | August 13, 1985 |
| K850711 | INHALATION THERAPY NEBULIZER DEVICE | June 5, 1985 |
| K841803 | A1 SYSTEME 8201/2 | February 25, 1985 |