FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODIFIED MODEL UA-711 DIGITAL SPHYGMONOMETER

K Number: K871718 · Decision Jun 24, 1987
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
76
Applicant Total
34
Review Days
51

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Basic Information

Device Name
MODIFIED MODEL UA-711 DIGITAL SPHYGMONOMETER
K Number
K871718
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1110
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
A&D Engineering, Inc.
Date Received
May 4, 1987
Decision Date
June 24, 1987
Product Code
DSK
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSK Computer, Blood-Pressure

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Other Clearances by A&D Engineering, Inc.

K Number Device Name
K082734 A&D MEDICAL UA-851THW DIGITAL BLOOD PRESSURE MONITOR
K062027 A&D MEDICAL UA-789 DIGITAL BLOOD PRESSURE MONITOR
K061456 A & D MEDICAL UM-101 DIGITAL BLOOD PRESSURE MONITOR
K043217 A&D MEDICAL UA-767PBT DIGITAL BLOOD PRESSURE MONITOR
K042967 A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512
K040371 A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR
K040229 A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODEL UB-328
K032499 A & D MEDICAL LIFESOURCE UA-704 DIGITAL BLOOD PRESSURE MONITORS
K012472 A & D MEDICAL LIFESOURCE UA-781, UA781PC, & UA-781T DIGITAL BLOOD PRESSURE MONITORS
K012013 LIFESOURCE MODELS UA-787, UA 787PC, UA-787T
Search all 34 clearances from A&D Engineering, Inc. →