Electromek Diagnostic Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electromek Diagnostic Systems, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Electromek Diagnostic Systems, Inc. has 11 FDA 510(k) cleared radiology devices. Based in Troy, US.
Historical record: 11 cleared submissions from 1990 to 1991.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Electromek Diagnostic Systems, Inc.
11 devices
Cleared
Feb 13, 1991
G.E. DXD 325/350/350II/DXD 525/525II GENERATORS
Radiology
232d
Cleared
Dec 26, 1990
G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS
Radiology
183d
Cleared
Dec 19, 1990
G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN
Radiology
176d
Cleared
Dec 19, 1990
G.E. MSI 850/850II/1250 THREE PHASE GENERATORS
Radiology
176d
Cleared
Nov 13, 1990
G.E. POLARIX II C-ARM
Radiology
140d
Cleared
Nov 07, 1990
G.E. FLUOROCON 300 IMAGING SYSTEM
Radiology
134d
Cleared
Nov 06, 1990
SIEMEN'S SIREMOBILE II C-ARM
Radiology
133d
Cleared
Oct 29, 1990
G.E. 48-4 CEILING TUBEHANGER
Radiology
125d
Cleared
Oct 29, 1990
G.E. MONITROL 90 AND G.E. MONITROL 15
Radiology
125d
Cleared
Oct 26, 1990
G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS
Radiology
122d
Cleared
Oct 23, 1990
G.E. XT CEILING TUBE SUSPENSION
Radiology
119d