510(k) Report

FDA applicant

Thermoquest Corp.

Marietta, OH2 decisions1999–20000 recalls

FDA records 2 decisions for Thermoquest Corp. (Marietta, OH) from 1999 to 2000: 2 510(k) clearances. All are in product code MQG (Accessory, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Thermoquest Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thermoquest 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?

  • MQGAccessory, Assisted Reproduction2decisions

Who builds on its devices?

Later devices cite its devices 2 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.

  • K991408Forma Scientific Universal Water-Jacketed IncubatorThermoquest Corp. · 19991cites it
  • K001524Forma Scientific Direct Heat IncubatorsThermoquest Corp. · 20001cites it

What has FDA decided for it lately?

  • K001524Forma Scientific Direct Heat IncubatorsThermoquest Corp. · 2000
  • K991408Forma Scientific Universal Water-Jacketed IncubatorThermoquest Corp. · 1999

All 2 as Thermoquest Corp. →