TRAVEL PAL (MM-111B) /MEGA MOTION— 510(k) K060697

Name: FDA 510(k) clearance K060697
Creator: U.S. Food and Drug Administration
Published: 2006-04-11

Substantially Equivalent

Mega Motion, Inc.

FDA 510(k) clearance K060697 for TRAVEL PAL (MM-111B) /MEGA MOTION, Substantially Equivalent on 2006-04-11. Applicant: Mega Motion, Inc.. Device class: 2.

Clearance details

Applicant: Mega Motion, Inc.
Product code: Code INI
Device class: Class 2
Regulation: 21 CFR 890.3800
Advisory panel: Physical Medicine
Date received: 2006-03-16
Decision date: 2006-04-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Old Forge, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code INI

product code INI

Injury: 171
Other: 1
Total: 172

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.