Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

B.07 STAIRWAY CHAIRLIFT

K-Number: K024345 · 2003-02-26

Decision Date2003-02-26
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

B.07 STAIRWAY CHAIRLIFT is the device name listed in this FDA 510(k) record. The listed applicant is Services Industriels Savaria, Inc.. It received FDA 510(k) clearance on 2003-02-26 under 510(k) number K024345. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B.07 STAIRWAY CHAIRLIFT?

B.07 STAIRWAY CHAIRLIFT is a medical device that received FDA 510(k) clearance on 2003-02-26. The listed applicant is Services Industriels Savaria, Inc.. The 510(k) number is K024345.

When did B.07 STAIRWAY CHAIRLIFT receive FDA 510(k) clearance?

B.07 STAIRWAY CHAIRLIFT received FDA 510(k) clearance on 2003-02-26, under 510(k) number K024345.

Who is the listed applicant for B.07 STAIRWAY CHAIRLIFT?

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 B.07 STAIRWAY CHAIRLIFT?

The FDA product code for B.07 STAIRWAY CHAIRLIFT 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 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: 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.

↑