THE MULTILIFT
K-Number: K024346 · 2003-03-04
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Device Summary
Frequently Asked Questions
What is the THE MULTILIFT?
THE MULTILIFT is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Services Industriels Savaria, Inc.. The 510(k) number is K024346.
When did THE MULTILIFT receive FDA 510(k) clearance?
THE MULTILIFT received FDA 510(k) clearance on 2003-03-04, under 510(k) number K024346.
Who is the listed applicant for THE MULTILIFT?
The FDA 510(k) record lists Services Industriels Savaria, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE MULTILIFT?
The FDA product code for THE MULTILIFT 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 Services Industriels Savaria, 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: 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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