510(k) Report

FDA applicant

Packard Instrument Co., Inc.

Downers Grove, IL4 decisions1988–19920 recalls

FDA records 4 decisions for Packard Instrument Co., Inc. (Downers Grove, IL) from 1988 to 1992: 4 510(k) clearances. Most are in product codes JQW (Station, Pipetting And Diluting, For Clinical…) and JTC (Device, Microtiter Diluting/Dispensing). 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 Packard Instrument Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Packard Instrument Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JQWStation, Pipetting And Diluting, For Clinical Use2decisions
  • JTCDevice, Microtiter Diluting/Dispensing2decisions

What has FDA decided for it lately?

  • K924907Filtermate Universal HarvesterPackard Instrument Co., Inc. · 1992
  • K913664Rosys Models 100 and 200Packard Instrument Co., Inc. · 1991
  • K901808Micromate 196 Model A961960Packard Instrument Co., Inc. · 1990
  • K883749Probe (TM) Models 700 and 1000Packard Instrument Co., Inc. · 1988

All 4 as Packard Instrument Co., Inc. →