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FDA 510(k)

DAB WELDLESS WHEELCHAIR

K-Number: K944122 · 1994-09-13

Decision Date1994-09-13
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DAB WELDLESS WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Da Intl. , Ltd.. It received FDA 510(k) clearance on 1994-09-13 under 510(k) number K944122. 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 DAB WELDLESS WHEELCHAIR?

DAB WELDLESS WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1994-09-13. The listed applicant is Da Intl. , Ltd.. The 510(k) number is K944122.

When did DAB WELDLESS WHEELCHAIR receive FDA 510(k) clearance?

DAB WELDLESS WHEELCHAIR received FDA 510(k) clearance on 1994-09-13, under 510(k) number K944122.

Who is the listed applicant for DAB WELDLESS WHEELCHAIR?

The FDA 510(k) record lists Da Intl. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAB WELDLESS WHEELCHAIR?

The FDA product code for DAB WELDLESS 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.

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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