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Mettler Electronics Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
32
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K113017SYS*STIM 240June 26, 2012
K111482SONICATOR PLUS 920August 25, 2011
K091540MTD 4000October 8, 2009
K071137SONICATOR PLUS 940, MODEL ME940August 1, 2007
K053546SONICATOR 740, MODEL ME 740May 4, 2006
K043586LASER SYS*STIM 540, MODEL ME 540May 6, 2005
K042554AUTO THERM 390, MODEL ME 390October 8, 2004
K031017SYS*STIM 208 AND 208AMay 30, 2003
K023083SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800February 28, 2003
K022458AUTO*THERM 395, MODEL ME 395September 26, 2002
K013192SONICATOR PLUS 930, MODEL ME 930October 17, 2001
K984142SONICATOR PLUS 992, MODEL NUMBER ME 992 AND SONICATOR PLUS 994, MODEL NUMBER ME 994February 9, 1999
K984114SYS STIM 294, MODEL ME 294February 9, 1999
K964028SYS STIM 226February 3, 1997
K951916CC RIDER, MODEL ME180October 4, 1995
K943469SONICATOR 730August 29, 1994
K934846SONICATOR 716March 23, 1994
K934845SONICATOR 715January 21, 1994
K921436SONICATOR PLUSApril 27, 1993
K893878SYS*STIM 206ADecember 19, 1989