Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

A&D Engineering, Inc. — Predicate Candidate Screening

34 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

84 daysmedian FDA review time

197 days90th percentile

34clearances measured

K-number	Device	Applicant	Decided	Review days
K082734	A&D MEDICAL UA-851THW DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	2008-11-13	56
K062027	A&D MEDICAL UA-789 DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	2007-01-19	185
K061456	A & D MEDICAL UM-101 DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	2006-06-21	27
K043217	A&D MEDICAL UA-767PBT DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	2005-03-03	101
K042967	A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODE	A&D Engineering, Inc.	2004-12-03	36
K040371	A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	2004-05-19	92
K040229	A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODE	A&D Engineering, Inc.	2004-03-19	46
K032499	A & D MEDICAL LIFESOURCE UA-704 DIGITAL BLOOD PRESSURE MONIT	A&D Engineering, Inc.	2003-10-30	78
K012472	A & D MEDICAL LIFESOURCE UA-781, UA781PC, & UA-781T DIGITAL	A&D Engineering, Inc.	2002-02-15	197
K012013	LIFESOURCE MODELS UA-787, UA 787PC, UA-787T	A&D Engineering, Inc.	2001-07-13	15
K010828	DIGITAL BLOOD PRESSURE MONITORS, MODELS TM-2655, TM-2655P, &	A&D Engineering, Inc.	2001-03-29	9
K002061	A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR	A&D Engineering, Inc.	2001-01-19	197
K002115	A&D MEDICAL LIFESOURCE UB-401PC & UB-401 DIGITAL BLOOD PRESS	A&D Engineering, Inc.	2000-07-25	12
K993116	A&D MEDICAL UT-101 LIFESOURCE DIGITAL EAR THEROMETER	A&D Engineering, Inc.	2000-04-12	205
K993888	A & D MEDICALLIFESOURCE US-779PC & UA-779T DIGITAL BLOOD PRE	A&D Engineering, Inc.	1999-12-20	34
K982481	A&D MEDICAL UA-767PC DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	1998-09-25	71
K980824	A&D UB-322 WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	1998-03-19	15
K960319	A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	1996-07-02	161
K914273	A&D TM-2421/2021 AMBULATORY BLOOD PRESSURE MONITOR	A&D Engineering, Inc.	1993-02-09	504
K912119	DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212	A&D Engineering, Inc.	1991-08-07	85
K912118	DIGITAL SPHYGMOMANOMETER MODEL UA-833	A&D Engineering, Inc.	1991-08-07	85
K911049	DIGITAL SPHYGMOIMANOMETER, MODEL UA-830	A&D Engineering, Inc.	1991-08-07	152
K895428	A&D AUTOMATIC DIGITAL BLOOD PRESSURE METER 2510/20	A&D Engineering, Inc.	1989-11-28	84
K895429	A&D AUTOMATIC DIGITAL BLOOD PRESSURE METER 2650	A&D Engineering, Inc.	1989-11-28	84
K882824	TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR	A&D Engineering, Inc.	1989-01-17	193
K882825	TAKEDA MEDICAL AUTO. DIG. BLOOD PRES. METER W/PRIN	A&D Engineering, Inc.	1989-01-17	193
K880079	TAKEDA MEDICAL AUTO. AMBU. BLOOD PRESS. METER/2420	A&D Engineering, Inc.	1988-03-31	80
K874338	TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2610	A&D Engineering, Inc.	1988-02-05	107
K874339	TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620	A&D Engineering, Inc.	1987-12-18	58
K872629	TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER/ UA-741	A&D Engineering, Inc.	1987-09-15	71
K871720	MODIFIED MODEL UA-731 DIGITAL SPHYGMOMANOMETER	A&D Engineering, Inc.	1987-07-29	86
K871718	MODIFIED MODEL UA-711 DIGITAL SPHYGMONOMETER	A&D Engineering, Inc.	1987-06-24	51
K871719	MODIFIED MODEL UA-751 DIGITAL SPHYGMONOMETER	A&D Engineering, Inc.	1987-06-05	32
K870728	TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER UA-701	A&D Engineering, Inc.	1987-03-27	31

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda