Shenzhen Pango Electronic Co., Ltd.
Shanghai, CN
Shenzhen Pango Electronic Co., Ltd. appears in FDA device records in Shanghai, CN. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Shenzhen Pango Electronic Co., Ltd. between 2010 and 2021. The busiest year on record is 2010, with 2. The most recent is 2021, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 2 |
| 2013 | 2 |
| 2017 | 2 |
| 2019 | 1 |
| 2020 | 1 |
| 2021 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K203746 | Venen-trainer (Model: FM150, SFM90) | JOW | Substantially Equivalent | |
| K200716 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K182597 | Infrared thermometer | FLL | Substantially Equivalent | |
| K170151 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K161845 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | |
| K131558 | PG-800B SERIES, INCLUDING PG-800BD, PG-800B-1, PG-800BD-1, PG-800B3, PG-800B4, PG-800B4D, PG-800B5, PG-800B5-1, PG-800B6 | DXN | Substantially Equivalent | |
| K131569 | PG-800A SERIES | DXN | Substantially Equivalent | |
| K102988 | ELECTRONIC BLOOD PRESURE MONITOR | DXN | Substantially Equivalent | |
| K102920 | ELECTRONIC BLOOD PRESSURE MONITOR | 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