FDA 510(k) Applications Submitted by MEDICAL INSTRUMENTS TECHNOLOGY, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K012614 |
08/13/2001 |
KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
K012624 |
08/13/2001 |
REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURS |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
K012632 |
08/13/2001 |
TOURNIQUET CUFF; PNEUMATIC TOURNIQUET |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
K012640 |
08/13/2001 |
ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS |
MEDICAL INSTRUMENTS TECHNOLOGY, INC. |
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