510(k) Report

FDA applicant

Mountain Medical Equipment, Inc.

Littleton, CO20 decisions1978–19950 recalls

FDA records 20 decisions for Mountain Medical Equipment, Inc. (Littleton, CO) from 1978 to 1995: 20 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and BTI (Compressor, Air, Portable). 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 Mountain Medical Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mountain Medical Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mountain Medical Equipment, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Mountain”

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