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FDA 510(k)

QUADRA WHEELCHAIR, QUADRA CHAIR, ETC.

K-Number: K801317 · 1980-07-21

Decision Date1980-07-21
Product CodeIQC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUADRA WHEELCHAIR, QUADRA CHAIR, ETC. is the device name listed in this FDA 510(k) record. The listed applicant is Quadra Wheelchairs, Inc.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801317. The device is classified under product code IQC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUADRA WHEELCHAIR, QUADRA CHAIR, ETC.?

QUADRA WHEELCHAIR, QUADRA CHAIR, ETC. is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Quadra Wheelchairs, Inc.. The 510(k) number is K801317.

When did QUADRA WHEELCHAIR, QUADRA CHAIR, ETC. receive FDA 510(k) clearance?

QUADRA WHEELCHAIR, QUADRA CHAIR, ETC. received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801317.

Who is the listed applicant for QUADRA WHEELCHAIR, QUADRA CHAIR, ETC.?

The FDA 510(k) record lists Quadra Wheelchairs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUADRA WHEELCHAIR, QUADRA CHAIR, ETC.?

The FDA product code for QUADRA WHEELCHAIR, QUADRA CHAIR, ETC. is IQC.

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.

Related Devices (Code: IQC)

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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