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FDA 510(k)

IURA UNIVERSAL WHEELCHAIR/STRETCHER-

K-Number: K840125 · 1984-01-27

Decision Date1984-01-27
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IURA UNIVERSAL WHEELCHAIR/STRETCHER- is the device name listed in this FDA 510(k) record. The listed applicant is Trade West, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K840125. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IURA UNIVERSAL WHEELCHAIR/STRETCHER-?

IURA UNIVERSAL WHEELCHAIR/STRETCHER- is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Trade West, Inc.. The 510(k) number is K840125.

When did IURA UNIVERSAL WHEELCHAIR/STRETCHER- receive FDA 510(k) clearance?

IURA UNIVERSAL WHEELCHAIR/STRETCHER- received FDA 510(k) clearance on 1984-01-27, under 510(k) number K840125.

Who is the listed applicant for IURA UNIVERSAL WHEELCHAIR/STRETCHER-?

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

What is the FDA product code for IURA UNIVERSAL WHEELCHAIR/STRETCHER-?

The FDA product code for IURA UNIVERSAL WHEELCHAIR/STRETCHER- is FPO.

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 Trade West, 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: FPO)

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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