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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