National Medical Technology
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K871668 | BIODAN TYPE COMET ELECTRODE | June 10, 1987 |
| K861158 | S&W TYPE 888 ELECTRODE | July 1, 1986 |
| K830888 | COOL-LITE FIBERCOPTIC LARYNGEAL EXAM | April 27, 1983 |
| K790845 | DUALUME LARYNGEAL EXAMINATION TELESCOPE | July 24, 1979 |