UNIVERSAL WHEELCHAIR
K-Number: K930411 · 1993-03-31
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Device Summary
Frequently Asked Questions
What is the UNIVERSAL WHEELCHAIR?
UNIVERSAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K930411.
When did UNIVERSAL WHEELCHAIR receive FDA 510(k) clearance?
UNIVERSAL WHEELCHAIR received FDA 510(k) clearance on 1993-03-31, under 510(k) number K930411.
Who is the listed applicant for UNIVERSAL WHEELCHAIR?
The FDA 510(k) record lists Everest & Jennings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIVERSAL WHEELCHAIR?
The FDA product code for UNIVERSAL 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.
Other records listing Everest & Jennings, 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: 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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