FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR
K-Number: K910752 · 1991-03-05
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Device Summary
Frequently Asked Questions
What is the FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR?
FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1991-03-05. The listed applicant is Fortress Litestyle. The 510(k) number is K910752.
When did FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR receive FDA 510(k) clearance?
FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR received FDA 510(k) clearance on 1991-03-05, under 510(k) number K910752.
Who is the listed applicant for FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR?
The FDA 510(k) record lists Fortress Litestyle as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR?
The FDA product code for FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIR is IOR.
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 Fortress Litestyle 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: IOR)
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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