510(k) Report

FDA applicant

Mediaid, Inc.

Cerritos, CA4 decisions2004–20080 recalls

FDA records 4 decisions for Mediaid, Inc. (Cerritos, CA) from 2004 to 2008: 4 510(k) clearances. All are in product code DQA (Oximeter). Its devices cite 16 predicates, 0 of them its own earlier devices. 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 Mediaid, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007: 22008: 1
2007high 2 (2007) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mediaid, 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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