FDA applicant
Aeroquip Medical Products
FDA records 2 decisions for Aeroquip Medical Products (Ann Arbor, MI) in 1997: 2 510(k) clearances. All are in product code FOZ (Catheter, Intravascular, Therapeutic…). 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 Aeroquip Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Aeroquip Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Aeroquip Medical Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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