510(k) Report

FDA applicant

Liquid Air Corp.

Walnut Creek, CA2 decisions1987–19900 recalls

FDA records 2 decisions for Liquid Air Corp. (Walnut Creek, CA) from 1987 to 1990: 2 510(k) clearances. All are in product code BXK (Gas, Calibration (Specified Concentration)). 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 Liquid Air Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Liquid Air Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Liquid Air 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

Other applicant names beginning “Liquid”

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