A&D Company, Ltd.
San Jose, CA, US
A&D Company, Ltd. appears in FDA device records in San Jose, CA. FDA records list 10 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for A&D Company, Ltd. between 2011 and 2022. The busiest year on record is 2014, with 3. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2011 | 1 |
| 2014 | 3 |
| 2016 | 1 |
| 2017 | 2 |
| 2019 | 2 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K212168 | A&D Medical UM-212BLE Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K173065 | A&D Medical Blood Pressure Monitors | DXN | Substantially Equivalent | |
| K173191 | A&D Medical Blood Pressure Monitors | DXN | Substantially Equivalent | |
| K170196 | A&D Medical UB-1100BLE UltraConnect Digital Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K163683 | A&D Medical UA-1200BLE UltraConnect Digital Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K151953 | A&D Medical TM-2657 Family of Digital Blood Pressure Monitors | DXN | Substantially Equivalent | |
| K141201 | A&D MEDICAL UA-767F AND UA-767FAC DIGITAL BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | |
| K141160 | A&D MEDICAL UA-651 DIGITAL BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | |
| K141179 | A&D MEDICAL UB-543 DIGITAL BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | |
| K111686 | A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS | DXN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain