BATTERY POWERED PATIENT LIFT
K-Number: K840997 · 1984-04-17
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Device Summary
Frequently Asked Questions
What is the BATTERY POWERED PATIENT LIFT?
BATTERY POWERED PATIENT LIFT is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Invacare Corp.. The 510(k) number is K840997.
When did BATTERY POWERED PATIENT LIFT receive FDA 510(k) clearance?
BATTERY POWERED PATIENT LIFT received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840997.
Who is the listed applicant for BATTERY POWERED PATIENT LIFT?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BATTERY POWERED PATIENT LIFT?
The FDA product code for BATTERY POWERED PATIENT LIFT is FSA.
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 Invacare Corp. 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: FSA)
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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