510(k) Report

FDA applicant

Micro Current Technology, Inc.

Seattle, WA8 decisions1999–20250 recalls

FDA records 8 decisions for Micro Current Technology, Inc. (Seattle, WA) from 1999 to 2025: 8 510(k) clearances. Most are in product codes NFO (Stimulator, Transcutaneous Electrical…) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Since 2016 its 510(k)s took a median of 86 days from receipt to decision, against 128 for FDA’s reviews in the same codes and years. 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, neurology panel, where it files most

How often FDA has decided Micro Current Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2018: 12019: 12023: 12024: 12025: 1
2007high 1 (2018) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micro Current Technology, Inc.’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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