Micromed Development Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micromed Development Corp. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Micromed Development Corp. has 14 FDA 510(k) cleared ear, nose, throat devices. Based in Clearwater, US.
Historical record: 14 cleared submissions from 1994 to 1996.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Micromed Development Corp.
14 devices
Cleared
May 14, 1996
POLY/PLATINUM WIRE PISTON
Ear, Nose, Throat
574d
Cleared
Jan 20, 1995
DISPOSABLE JOINT ASPIRATION/INJECTION DIAGNOSTIC KIT
General & Plastic Surgery
52d
Cleared
Dec 27, 1994
NERVE MONITOR ELECTRODES/STIMULATOR PROBES
Ear, Nose, Throat
61d
Cleared
Nov 22, 1994
MICROMED PARTIAL REGULAR AND PARTIAL OFFSET
Ear, Nose, Throat
35d
Cleared
Nov 22, 1994
MICROMED TOTAL REGULAR AND PARTIAL OFFSET
Ear, Nose, Throat
35d
Cleared
Nov 22, 1994
POLY-WIRE PISTON
Ear, Nose, Throat
35d
Cleared
Nov 22, 1994
POLY PISTON
Ear, Nose, Throat
35d
Cleared
Nov 22, 1994
EDI-BUR MICRODRILL SYSTEMS
Ear, Nose, Throat
33d
Cleared
Sep 16, 1994
COLLAR BUTTON VENTURI VENT TUBE
Ear, Nose, Throat
43d
Cleared
Sep 02, 1994
BOBBIN STYLE VENTURI VENT TUBE
Ear, Nose, Throat
29d
Cleared
Sep 02, 1994
GROMMENT STYLE VENTURI TUBE
Ear, Nose, Throat
29d
Cleared
Aug 24, 1994
C-FLEX VENT TUBES
Ear, Nose, Throat
50d