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FDA 510(k)

MODEL SEGAEGO 3D SCOOTER

K-Number: K071284 · 2007-07-26

ApplicantDalton Medical Corp.
Decision Date2007-07-26
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL SEGAEGO 3D SCOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Dalton Medical Corp.. It received FDA 510(k) clearance on 2007-07-26 under 510(k) number K071284. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL SEGAEGO 3D SCOOTER?

MODEL SEGAEGO 3D SCOOTER is a medical device that received FDA 510(k) clearance on 2007-07-26. The listed applicant is Dalton Medical Corp.. The 510(k) number is K071284.

When did MODEL SEGAEGO 3D SCOOTER receive FDA 510(k) clearance?

MODEL SEGAEGO 3D SCOOTER received FDA 510(k) clearance on 2007-07-26, under 510(k) number K071284.

Who is the listed applicant for MODEL SEGAEGO 3D SCOOTER?

The FDA 510(k) record lists Dalton Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL SEGAEGO 3D SCOOTER?

The FDA product code for MODEL SEGAEGO 3D SCOOTER is INI.

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Other records listing Dalton Medical Corp. as applicant

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Related Devices (Code: INI)

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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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