Howard Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 4
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K063104 | FOX MEDICAL DIODE LASER SYSTEM 810NM | May 16, 2007 |
| K030948 | VMATE MODEL VMM1000 | June 17, 2003 |
| K980985 | SCMD-1000 | May 1, 1998 |
| K974598 | MICROKERATOME OR THE MATE | April 22, 1998 |
| K972727 | CBALK-1000 BLADE | October 10, 1997 |