510(k) Report

FDA applicant

Mountain View Medical

Corona, CA2 decisions1985–19860 recalls

FDA records 2 decisions for Mountain View Medical (Corona, CA) from 1985 to 1986: 2 510(k) clearances. Most are in product codes DSI (Detector And Alarm, Arrhythmia) and DSH (Recorder, Magnetic Tape, Medical). 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, cardiovascular panel, where it files most

How often FDA has decided Mountain View Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mountain View Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mountain View Medical 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?

  • DSIDetector And Alarm, Arrhythmia1decision
  • DSHRecorder, Magnetic Tape, Medical1decision

What has FDA decided for it lately?

  • K861240Bechler Medical, Model 5000,the Wiz Holter ScannerMountain View Medical · 1986
  • K853985MVM 4000 Holter IV RecorderMountain View Medical · 1985

All 2 as Mountain View Medical →

Other applicant names beginning “Mountain”

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

Mountain Medical Equipment, Inc. 20Mountain Shades, Inc. 3Mountain Medico, Inc. 2Mountain Precision Mfg. Ltd. Co. 1