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FDA 510(k)

MECHANICAL WHEELCHAIR, MODEL DS 202-S

K-Number: K100824 · 2010-05-25

Decision Date2010-05-25
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MECHANICAL WHEELCHAIR, MODEL DS 202-S is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou KD Medical. It received FDA 510(k) clearance on 2010-05-25 under 510(k) number K100824. 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 MECHANICAL WHEELCHAIR, MODEL DS 202-S?

MECHANICAL WHEELCHAIR, MODEL DS 202-S is a medical device that received FDA 510(k) clearance on 2010-05-25. The listed applicant is Suzhou KD Medical. The 510(k) number is K100824.

When did MECHANICAL WHEELCHAIR, MODEL DS 202-S receive FDA 510(k) clearance?

MECHANICAL WHEELCHAIR, MODEL DS 202-S received FDA 510(k) clearance on 2010-05-25, under 510(k) number K100824.

Who is the listed applicant for MECHANICAL WHEELCHAIR, MODEL DS 202-S?

The FDA 510(k) record lists Suzhou KD Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MECHANICAL WHEELCHAIR, MODEL DS 202-S?

The FDA product code for MECHANICAL WHEELCHAIR, MODEL DS 202-S 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

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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