FDA applicant
Vitaphore Corp.
FDA records 13 decisions for Vitaphore Corp. (Menlo Park, CA) from 1986 to 1992: 13 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and KMK (Device, Intravascular Catheter Securement). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Vitaphore Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Vitaphore Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Vitaphore Corp.’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