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FDA 510(k)

CLEAN ROOM WHEELCHAIR

K-Number: K954328 · 1995-11-17

Decision Date1995-11-17
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLEAN ROOM WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Forth Research, Inc.. It received FDA 510(k) clearance on 1995-11-17 under 510(k) number K954328. 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 CLEAN ROOM WHEELCHAIR?

CLEAN ROOM WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1995-11-17. The listed applicant is Forth Research, Inc.. The 510(k) number is K954328.

When did CLEAN ROOM WHEELCHAIR receive FDA 510(k) clearance?

CLEAN ROOM WHEELCHAIR received FDA 510(k) clearance on 1995-11-17, under 510(k) number K954328.

Who is the listed applicant for CLEAN ROOM WHEELCHAIR?

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

What is the FDA product code for CLEAN ROOM WHEELCHAIR?

The FDA product code for CLEAN ROOM 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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