510(k) Report

FDA applicant

Jtl Medical Corp.

Riverside, CA3 decisions1991–19930 recalls

FDA records 3 decisions for Jtl Medical Corp. (Riverside, CA) from 1991 to 1993: 3 510(k) clearances. Most are in product codes DTW (Monitor And/Or Control, Level Sensing…) and DWF (Catheter, Cannula And Tubing, Vascular…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Jtl Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jtl Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jtl Medical Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Jtl Medical Corp.’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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