HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT
K-Number: K893544 · 1989-06-12
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Device Summary
Frequently Asked Questions
What is the HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT?
HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is The Cheney Co.. The 510(k) number is K893544.
When did HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT receive FDA 510(k) clearance?
HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT received FDA 510(k) clearance on 1989-06-12, under 510(k) number K893544.
Who is the listed applicant for HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT?
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 HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT?
The FDA product code for HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT is ING.
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: ING)
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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