Innotron Diagnostics
FDA Regulatory Profile
Innotron Diagnostics appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 12, 1985.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K850629 | INNOFLUOR THEOPHYLLINE | March 12, 1985 |
| K844721 | INNOFLUOR PRIMIDONE | January 8, 1985 |
| K841866 | INNOFLOUR TOBRAMYCIN | May 31, 1984 |
| K841865 | INNOFLOUR GENTAMICIN | May 31, 1984 |
| K841707 | INNOFLUOR PHENOBARBITAL | May 23, 1984 |
| K841706 | INNOFLUOR PHENYTOIN | May 22, 1984 |