Mettler Electronics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mettler Electronics Corp. - FDA 510(k) Cleared Devices
32
Total
28
Cleared
0
Denied
Mettler Electronics Corp. has 28 FDA 510(k) cleared physical medicine devices. Based in Anaheim, US.
Historical record: 28 cleared submissions from 1985 to 2012.
Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mettler Electronics Corp.
32 devices
Cleared
Jun 26, 2012
SYS*STIM 240
Physical Medicine
259d
Cleared
Aug 25, 2011
SONICATOR PLUS 920
Physical Medicine
90d
Cleared
Oct 08, 2009
MTD 4000
Physical Medicine
135d
Cleared
Aug 01, 2007
SONICATOR PLUS 940, MODEL ME940
Physical Medicine
99d
Cleared
May 04, 2006
SONICATOR 740, MODEL ME 740
Physical Medicine
135d
Cleared
May 06, 2005
LASER SYS*STIM 540, MODEL ME 540
Physical Medicine
129d
Cleared
Oct 08, 2004
AUTO THERM 390, MODEL ME 390
Physical Medicine
18d
Cleared
May 30, 2003
SYS*STIM 208 AND 208A
Physical Medicine
60d
Cleared
Feb 28, 2003
SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800
General Hospital
164d
Cleared
Sep 26, 2002
AUTO*THERM 395, MODEL ME 395
Physical Medicine
62d
Cleared
Oct 17, 2001
SONICATOR PLUS 930, MODEL ME 930
Physical Medicine
22d
Cleared
Feb 09, 1999
SYS STIM 294, MODEL ME 294
Physical Medicine
84d