510(k) Report

FDA applicant

Prisma Systems

Rome, NY27 decisions1994–19950 recalls

FDA records 27 decisions for Prisma Systems (Rome, NY) from 1994 to 1995: 27 510(k) clearances. Most are in product codes CIG (Diazo Colorimetry, Bilirubin) and CIT (Nadh Oxidation/Nad Reduction, Ast/Sgot). 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 Prisma Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Prisma Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Prisma Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report