510(k) Report

FDA applicant

Chemfet Corp.

Bellevue, WA3 decisions1987–19870 recalls

FDA records 3 decisions for Chemfet Corp. (Bellevue, WA) in 1987: 3 510(k) clearances. Most are in product codes FFT (Electrode, Ph, Stomach) and IKD (Cable, Electrode). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Chemfet Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Chemfet 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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