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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