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FDA 510(k)

STAINLESS STEEL AQUATIC WHEELCHAIR

K-Number: K031910 · 2003-07-25

Decision Date2003-07-25
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAINLESS STEEL AQUATIC WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Db Perks & Associates , Ltd.. It received FDA 510(k) clearance on 2003-07-25 under 510(k) number K031910. 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 STAINLESS STEEL AQUATIC WHEELCHAIR?

STAINLESS STEEL AQUATIC WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2003-07-25. The listed applicant is Db Perks & Associates , Ltd.. The 510(k) number is K031910.

When did STAINLESS STEEL AQUATIC WHEELCHAIR receive FDA 510(k) clearance?

STAINLESS STEEL AQUATIC WHEELCHAIR received FDA 510(k) clearance on 2003-07-25, under 510(k) number K031910.

Who is the listed applicant for STAINLESS STEEL AQUATIC WHEELCHAIR?

The FDA 510(k) record lists Db Perks & Associates , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAINLESS STEEL AQUATIC WHEELCHAIR?

The FDA product code for STAINLESS STEEL AQUATIC 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

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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