IURA UNIVERSAL WHEELCHAIR/STRETCHER-
K-Number: K840125 · 1984-01-27
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Device Summary
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
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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