Sichuan Prius Biotechnology Co., Ltd.
Yibin, CN
Sichuan Prius Biotechnology Co., Ltd. appears in FDA device records in Yibin, 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 Sichuan Prius Biotechnology Co., Ltd. between 2021 and 2022. The busiest year on record is 2022, with 8. The most recent is 2022, with 8.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2021 | 1 |
| 2022 | 8 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K221078 | Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use | FPA | Substantially Equivalent | |
| K221075 | Infusion Sets for Single Use | FPA | Substantially Equivalent | |
| K221069 | Infusion Sets for Single Use with Needles | FPA | Substantially Equivalent | |
| K221080 | Sterile Safety Hypodermic Needles for Single Use | FMI | Substantially Equivalent | |
| K221079 | Sterile Hypodermic Syringes for Single Use | FMF | Substantially Equivalent | |
| K221073 | Sterile Hypodermic Syringes for Single Use with Safety Needles | MEG | Substantially Equivalent | |
| K221068 | Sterile Hypodermic Syringes for Single Use with Needles | FMF | Substantially Equivalent | |
| K221066 | Sterile Hypodermic Needles for Single Use | FMI | Substantially Equivalent | |
| K210908 | Surgical Mask | FXX | 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