510(k) Report

FDA applicant

The Perkin-Elmer Corp.

Mchenry, IL62 decisions1976–19940 recalls

FDA records 62 decisions for The Perkin-Elmer Corp. (Mchenry, IL) from 1976 to 1994: 62 510(k) clearances. Most are in product codes JXR (Atomic Absorption Spectrophotometer, General Use) and KHO (Fluorometer, For Clinical Use). 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 The Perkin-Elmer Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Perkin-Elmer Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Perkin-Elmer Corp.’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