FDA applicant
Precision Med Products, Ltd.
FDA records 16 decisions for Precision Med Products, Ltd. (Marrtinsville, IN) in 1993: 16 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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 Precision Med Products, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Precision Med Products, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Precision Med Products, Ltd.’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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