TRAVEL PAL (MM-111B) /MEGA MOTION
K-Number: K060697 · 2006-04-11
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Device Summary
Frequently Asked Questions
What is the TRAVEL PAL (MM-111B) /MEGA MOTION?
TRAVEL PAL (MM-111B) /MEGA MOTION is a medical device that received FDA 510(k) clearance on 2006-04-11. The listed applicant is Mega Motion, Inc.. The 510(k) number is K060697.
When did TRAVEL PAL (MM-111B) /MEGA MOTION receive FDA 510(k) clearance?
TRAVEL PAL (MM-111B) /MEGA MOTION received FDA 510(k) clearance on 2006-04-11, under 510(k) number K060697.
Who is the listed applicant for TRAVEL PAL (MM-111B) /MEGA MOTION?
The FDA 510(k) record lists Mega Motion, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAVEL PAL (MM-111B) /MEGA MOTION?
The FDA product code for TRAVEL PAL (MM-111B) /MEGA MOTION is INI.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Mega Motion, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: INI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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