510(k) Report

FDA applicant

Sfri, Inc.

Irvine, CA1 decision1998–19980 recalls

FDA records 1 decision for Sfri, Inc. (Irvine, CA) in 1998: 1 510(k) clearance. All are in product code JJQ (Colorimeter, Photometer, Spectrophotometer For…). 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 Sfri, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sfri, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sfri, 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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