Medical Instruments Technology, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K012614 | KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN | May 1, 2002 |
| K012640 | ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS | February 28, 2002 |
| K012624 | REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ART | November 8, 2001 |
| K012632 | TOURNIQUET CUFF; PNEUMATIC TOURNIQUET | October 26, 2001 |
| K884611 | THE ORTHORANGER II ELECTRONIC GONIOMETER | January 31, 1989 |