LIBERTY SPECIAL AND LIBERTY STAIRLIFTS
K-Number: K896628 · 1990-01-12
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Device Summary
Frequently Asked Questions
What is the LIBERTY SPECIAL AND LIBERTY STAIRLIFTS?
LIBERTY SPECIAL AND LIBERTY STAIRLIFTS is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is The Cheney Co.. The 510(k) number is K896628.
When did LIBERTY SPECIAL AND LIBERTY STAIRLIFTS receive FDA 510(k) clearance?
LIBERTY SPECIAL AND LIBERTY STAIRLIFTS received FDA 510(k) clearance on 1990-01-12, under 510(k) number K896628.
Who is the listed applicant for LIBERTY SPECIAL AND LIBERTY STAIRLIFTS?
The FDA 510(k) record lists The Cheney Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIBERTY SPECIAL AND LIBERTY STAIRLIFTS?
The FDA product code for LIBERTY SPECIAL AND LIBERTY STAIRLIFTS is ILK.
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 The Cheney Co. 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: ILK)
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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