FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MTD 4000

K Number: K091540 · Decision Oct 8, 2009
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
70
Applicant Total
32
Review Days
135

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Basic Information

Device Name
MTD 4000
K Number
K091540
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
890.5900
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mettler Electronics Corp.
Date Received
May 26, 2009
Decision Date
October 8, 2009
Product Code
ITH
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ITH Equipment, Traction, Powered

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Other Clearances by Mettler Electronics Corp.

K Number Device Name
K113017 SYS*STIM 240
K111482 SONICATOR PLUS 920
K071137 SONICATOR PLUS 940, MODEL ME940
K053546 SONICATOR 740, MODEL ME 740
K043586 LASER SYS*STIM 540, MODEL ME 540
K042554 AUTO THERM 390, MODEL ME 390
K031017 SYS*STIM 208 AND 208A
K023083 SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800
K022458 AUTO*THERM 395, MODEL ME 395
K013192 SONICATOR PLUS 930, MODEL ME 930
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