Medical Device Manufacturer · US , Clearwater , FL

Mercury Medical - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1994
15
Total
15
Cleared
0
Denied

Mercury Medical has 15 FDA 510(k) cleared anesthesiology devices. Based in Clearwater, US.

Historical record: 15 cleared submissions from 1994 to 2014.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mercury Medical
15 devices
1-15 of 15
Cleared Oct 17, 2014
T-PIECE RESUSCITATOR
K142096 · BTL
Anesthesiology · 77d
Cleared Aug 20, 2009
MERCURY CPAP
K090710 · BYE
Anesthesiology · 155d
Cleared Feb 23, 2009