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FDA 510(k) Applications Submitted by MICRO WEISS ELECTRONICS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970139
01/15/1997
MICROLIFE MANUAL BLOOD PRESSURE MONITOR (MANUAL INFLATE) MODEL BP-2BIO
MICRO WEISS ELECTRONICS
K970211
01/21/1997
MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR
MICRO WEISS ELECTRONICS
K972259
06/17/1997
PRO CHECK DIGITAL PACIFIER THERMOMETER
MICRO WEISS ELECTRONICS
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