510(k) Report

FDA applicant

Par Microsystems Corp.

New Hartford, NY2 decisions1987–19930 recalls

FDA records 2 decisions for Par Microsystems Corp. (New Hartford, NY) from 1987 to 1993: 2 510(k) clearances. Most are in product codes HLQ (Keratoscope, Ac-Powered) and DSF (Recorder, Paper Chart). 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, ophthalmic panel, where it files most

How often FDA has decided Par Microsystems Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Par Microsystems Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Par Microsystems Corp. 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?

  • HLQKeratoscope, Ac-Powered1decision
  • DSFRecorder, Paper Chart1decision

Who builds on its devices?

Later devices cite its devices 5 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K870039Imagenet Digital Ophthalmic Imaging SystemPar Microsystems Corp. · 19875cite it

What has FDA decided for it lately?

  • K923435Corneal Topography SystemPar Microsystems Corp. · 1993
  • K870039Imagenet Digital Ophthalmic Imaging SystemPar Microsystems Corp. · 1987

All 2 as Par Microsystems Corp. →