K241322
- 510(k) number
- K241322
- Device name
- Electric Breast Pump (LD-208L, LD-3010L, LD-2010L, LD-3010, LD-2010)
- Applicant
- Joytech Healthcare Co. , Ltd. CN
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2024-12-19
- Date received
- 2024-05-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K241322.pdf
Official FDA record: K241322
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.