PREMIER 2 WHEELCHAIR
K-Number: K930412 · 1993-03-31
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Device Summary
Frequently Asked Questions
What is the PREMIER 2 WHEELCHAIR?
PREMIER 2 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 K930412.
When did PREMIER 2 WHEELCHAIR receive FDA 510(k) clearance?
PREMIER 2 WHEELCHAIR received FDA 510(k) clearance on 1993-03-31, under 510(k) number K930412.
Who is the listed applicant for PREMIER 2 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 PREMIER 2 WHEELCHAIR?
The FDA product code for PREMIER 2 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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