FDA applicant
Oem Medical Div.
FDA records 5 decisions for Oem Medical Div. (Richmond, VA) from 1977 to 1993: 5 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and GCX (Apparatus, Suction, Operating-Room, Wall…). 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 Oem Medical Div.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Oem Medical Div. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Oem Medical Div.’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