K242126
- 510(k) number
- K242126
- Device name
- I.V. Administration Set
- Applicant
- Bq Plus Medical Co., Ltd. CN
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2024-08-22
- Date received
- 2024-07-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K242126
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.