Data / Medical devices / United States / International Filter Products Dba Ifp Medical
International Filter Products Dba Ifp Medical: FDA-registered device maker in Sun Valley, CA, United States, 2 510(k) clearances
International Filter Products Dba Ifp Medical is registered with the FDA (registration 3030989877) in Sun Valley, CA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 18, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030989877
- Address
- 7914 Ajay Dr, Sun Valley, CA, United States, 91352
- Owner or operator
- International Filter Products DBA IFP Medical (10092402)
- Roles
- Complaint file establishment, Repackager or relabeler
- First device listed
- January 2, 2025
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, I.V. | KPE | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 18, 2023 | K223645 | I.V. Administration Set, I.V. Extension Set | FPA | Substantially Equivalent | Bq Plus Medical Co., Ltd. | accessdata.fda.gov |
| February 15, 2019 | K181393 | Empty Eva Bag, models FVM0134BP, FVM0135BP, FVM0136BP, FVM0137BP, FVM0138BP, FVM0139BP, FVM0140BP, FVM0141BP | KPE | Substantially Equivalent | Valmed S.R.L. | accessdata.fda.gov |
Compare with other makers
Updated May 18, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.