Microaire Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Microaire Surgical Instruments, Inc. has 4 FDA 510(k) cleared medical devices. Based in Charlottesville, US.
Historical record: 4 cleared submissions from 1996 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Microaire Surgical Instruments, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Mar 05, 2002
MICROAIRE 1000E SYSTEM
Neurology
85d
Cleared
Dec 10, 1998
LIGHT DUTY PNEUMATIC INSTRUMENT MODEL NUMBER PAD-100, HEAVY DUTY PNEUMATIC...
General & Plastic Surgery
192d
Cleared
Nov 26, 1997
MICROAIRE POWER ASPIRATION DEVICE PAD SYSTEM
General & Plastic Surgery
89d
Cleared
Jan 18, 1996
MICROAIRE SMARTDRIVE SYSTEM
Orthopedic
42d