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FDA 510(k)

STANDARD WHEELCHAIR

K-Number: K842719 · 1984-07-25

Decision Date1984-07-25
Product CodeIQC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STANDARD WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Greene International Corp.. It received FDA 510(k) clearance on 1984-07-25 under 510(k) number K842719. 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 STANDARD WHEELCHAIR?

STANDARD WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1984-07-25. The listed applicant is Greene International Corp.. The 510(k) number is K842719.

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

STANDARD WHEELCHAIR received FDA 510(k) clearance on 1984-07-25, under 510(k) number K842719.

Who is the listed applicant for STANDARD WHEELCHAIR?

The FDA 510(k) record lists Greene International Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STANDARD WHEELCHAIR?

The FDA product code for STANDARD WHEELCHAIR 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.

Other records listing Greene International Corp. 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: 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

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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