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FDA 510(k)

BRODA MODEL 587 MANUAL WHEELCHAIR

K-Number: K032133 · 2003-07-21

Decision Date2003-07-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BRODA MODEL 587 MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Broda Ent., Inc.. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K032133. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRODA MODEL 587 MANUAL WHEELCHAIR?

BRODA MODEL 587 MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is Broda Ent., Inc.. The 510(k) number is K032133.

When did BRODA MODEL 587 MANUAL WHEELCHAIR receive FDA 510(k) clearance?

BRODA MODEL 587 MANUAL WHEELCHAIR received FDA 510(k) clearance on 2003-07-21, under 510(k) number K032133.

Who is the listed applicant for BRODA MODEL 587 MANUAL WHEELCHAIR?

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

What is the FDA product code for BRODA MODEL 587 MANUAL WHEELCHAIR?

The FDA product code for BRODA MODEL 587 MANUAL WHEELCHAIR is IOR.

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 Broda Ent., 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: IOR)

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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