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FDA 510(k)

WHEELCHAIR ACCESSORIES

K-Number: K780184 · 1978-02-13

Decision Date1978-02-13
Product CodeIMX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-02-13 under 510(k) number K780184. The device is classified under product code IMX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR ACCESSORIES?

WHEELCHAIR ACCESSORIES is a medical device that received FDA 510(k) clearance on 1978-02-13. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780184.

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

WHEELCHAIR ACCESSORIES received FDA 510(k) clearance on 1978-02-13, under 510(k) number K780184.

Who is the listed applicant for WHEELCHAIR ACCESSORIES?

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

What is the FDA product code for WHEELCHAIR ACCESSORIES?

The FDA product code for WHEELCHAIR ACCESSORIES is IMX.

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 Orthopedic Equipment Co., 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.

View all 45 devices →

Related Devices (Code: IMX)

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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