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FDA 510(k)

WHEELCHAIR CONVERSION KIT

K-Number: K904650 · 1991-05-21

Decision Date1991-05-21
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR CONVERSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Hadco Marketing Services, Inc.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K904650. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR CONVERSION KIT?

WHEELCHAIR CONVERSION KIT is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Hadco Marketing Services, Inc.. The 510(k) number is K904650.

When did WHEELCHAIR CONVERSION KIT receive FDA 510(k) clearance?

WHEELCHAIR CONVERSION KIT received FDA 510(k) clearance on 1991-05-21, under 510(k) number K904650.

Who is the listed applicant for WHEELCHAIR CONVERSION KIT?

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

What is the FDA product code for WHEELCHAIR CONVERSION KIT?

The FDA product code for WHEELCHAIR CONVERSION KIT is ITI.

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 Hadco Marketing Services, 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: ITI)

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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