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FDA 510(k)

FOLDING WHEELCHAIR

K-Number: K915108 · 1992-01-13

Decision Date1992-01-13
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FOLDING WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Guardian Products Co., Inc.. It received FDA 510(k) clearance on 1992-01-13 under 510(k) number K915108. 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 FOLDING WHEELCHAIR?

FOLDING WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K915108.

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

FOLDING WHEELCHAIR received FDA 510(k) clearance on 1992-01-13, under 510(k) number K915108.

Who is the listed applicant for FOLDING WHEELCHAIR?

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

What is the FDA product code for FOLDING WHEELCHAIR?

The FDA product code for FOLDING 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 Guardian Products 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 8 devices →

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

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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