FDA applicant
Myron L Company
FDA records 1 decision for Myron L Company (Carlsbad, CA) in 2010: 1 510(k) clearance. All are in product code FLB (Meter, Conductivity, Induction, Remote Type). 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 Myron L Company’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2010high 1 (2010) · low 0 (2011)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Myron L Company’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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