FDA 510(k) Applications Submitted by SEIN ELECTRONICS CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K952826 06/20/1995 FULL AUTO FUZZY BLOOD PRESSURE METER MODEL SE-7000 SEIN ELECTRONICS CO., LTD.
K952827 06/20/1995 FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 SEIN ELECTRONICS CO., LTD.
K973078 08/18/1997 WRIST BLOOD PRESSURE METER MODEL SE-330 SEIN ELECTRONICS CO., LTD.
K042014 07/27/2004 DIGITAL BLOOD PRESSURE MONITOR, MODELS SE-9000, SE-9200 AND SE-9400 SEIN ELECTRONICS CO., LTD.
K052108 08/03/2005 SEIN BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM, MODEL BGP-100 SEIN ELECTRONICS CO., LTD.
K042138 08/09/2004 FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR MODEL# SE-311 SEIN ELECTRONICS CO., LTD.
K032927 09/22/2003 FULL AUTO ARM DIGITAL BLOOD PRESSURE MONITOR SEIN ELECTRONICS CO., LTD.
K991397 04/21/1999 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR SE-30 TENS SEIN ELECTRONICS CO., LTD.
K003282 10/19/2000 FULL AUTO BLOOD PRESSURE MONITOR, MODEL SE-7700H SEIN ELECTRONICS CO., LTD.
K003711 12/01/2000 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM, MODEL SE-25M/25P SEIN ELECTRONICS CO., LTD.
K012054 07/02/2001 FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL SE-312 SEIN ELECTRONICS CO., LTD.


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