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FDA 510(k) Applications Submitted by MSB LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K955261
11/09/1995
NEUTRALECT ADULT STANDARD, RETURN (REM) & PAEDIATRIC ELECTROSURGERY PLATE (MODIFICATION)
MSB LTD.
K944496
09/13/1994
BIOTRACE-N, NS, 410 AND RT
MSB LTD.
K944497
09/13/1994
UNILECT, MONITAB AND BIOTRACE-HR
MSB LTD.
K980229
01/22/1998
MSB TENS ELECTRODES (DISPOSABLE)
MSB LTD.
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