TRAVONEB MODEL # TONE 1— 510(k) K854747

Name: FDA 510(k) clearance K854747
Creator: U.S. Food and Drug Administration
Published: 1986-02-24

Substantially Equivalent

Travomed, Inc.

FDA 510(k) clearance K854747 for TRAVONEB MODEL # TONE 1, Substantially Equivalent on 1986-02-24. Applicant: Travomed, Inc.. Device class: 2.

Clearance details

Applicant: Travomed, Inc.
Product code: Code BTI
Device class: Class 2
Regulation: 21 CFR 868.6250
Advisory panel: Anesthesiology
Date received: 1985-11-26
Decision date: 1986-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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K864127 — MECHANICAL OXYGEN REGULATOR1986-11-13
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Adverse events under product code BTI

product code BTI

Death: 25
Malfunction: 1,168
Total: 1,193

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.