FDA applicant

Harris Calorific

Walker, MI2 decisions1979–19810 recalls

FDA records 2 decisions for Harris Calorific (Walker, MI) from 1979 to 1981: 2 510(k) clearances. Most are in product codes CAN (Regulator, Pressure, Gas Cylinder) and CAX (Flowmeter, Tube, Thorpe, Back-Pressure…). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Harris Calorific since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Harris”

FDA records each applicant name separately; these may or may not be the same firm.

Harris-Lake, Inc. 7 Harris Mfg. Co. 2 Harris Medical, LLC 1

Harris Calorific

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Harris”