Medical Instruments Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: KENDALL, SEQUENTIAL COMPRESSION DEVICE, ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS, REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURS
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medical Instruments Technology, Inc. General & Plastic Surgery ✕
1 devices