AMIGO GRAND TOUR
K-Number: K952112 · 1995-08-11
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Device Summary
Frequently Asked Questions
What is the AMIGO GRAND TOUR?
AMIGO GRAND TOUR is a medical device that received FDA 510(k) clearance on 1995-08-11. The listed applicant is Amigo Mobility Intl., Inc.. The 510(k) number is K952112.
When did AMIGO GRAND TOUR receive FDA 510(k) clearance?
AMIGO GRAND TOUR received FDA 510(k) clearance on 1995-08-11, under 510(k) number K952112.
Who is the listed applicant for AMIGO GRAND TOUR?
The FDA 510(k) record lists Amigo Mobility Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMIGO GRAND TOUR?
The FDA product code for AMIGO GRAND TOUR 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 Amigo Mobility Intl., 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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