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FDA 510(k)

WHEELCHAIR ELEVATOR

K-Number: K960276 · 1996-04-01

Decision Date1996-04-01
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR ELEVATOR 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 1996-04-01 under 510(k) number K960276. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR ELEVATOR?

WHEELCHAIR ELEVATOR is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Services Industriels Savaria, Inc.. The 510(k) number is K960276.

When did WHEELCHAIR ELEVATOR receive FDA 510(k) clearance?

WHEELCHAIR ELEVATOR received FDA 510(k) clearance on 1996-04-01, under 510(k) number K960276.

Who is the listed applicant for WHEELCHAIR ELEVATOR?

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 WHEELCHAIR ELEVATOR?

The FDA product code for WHEELCHAIR ELEVATOR 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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