510(k) Report

FDA applicant

Sen Tech Medical Corp.

Arden Hills, MN5 decisions1984–19910 recalls

FDA records 5 decisions for Sen Tech Medical Corp. (Arden Hills, MN) from 1984 to 1991: 5 510(k) clearances. Most are in product codes CEM (Electrode, Ion Specific, Potassium) and GET (Motor, Surgical Instrument, Pneumatic Powered). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Sen Tech Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sen Tech 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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