FDA applicant
International Medical Products, Inc.
FDA records 10 decisions for International Medical Products, Inc. (Minneapolis, MN) from 1986 to 1998: 10 510(k) clearances. Most are in product codes KPO (Dialysate Concentrate For Hemodialysis (Liquid…) and BSK (Cuff, Tracheal Tube, Inflatable). Its devices cite 2 predicates, 0 of them its own earlier devices. 3 recalls are linked to its devices.
FDA’s records also spell it “International Medical Products B.V.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided International Medical Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for International Medical Products, Inc. since 2007.
Recalls per year
1in 2018
Class I Class II/III not classified
Planning a device like International Medical Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report