The following data is part of a premarket notification filed by A & D Engineering, Inc. with the FDA for A & D Medical Um-101 Digital Blood Pressure Monitor.
Device ID | K061456 |
510k Number | K061456 |
Device Name: | A & D MEDICAL UM-101 DIGITAL BLOOD PRESSURE MONITOR |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | A & D ENGINEERING, INC. 1555 MCCANDLESS DR. Milpitas, CA 95035 |
Contact | Jerry Wang |
Correspondent | Jerry Wang A & D ENGINEERING, INC. 1555 MCCANDLESS DR. Milpitas, CA 95035 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-05-25 |
Decision Date | 2006-06-21 |
Summary: | summary |