TEMPEST ELECTRIC WHEELCHAIR
K-Number: K904958 · 1990-11-26
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Device Summary
Frequently Asked Questions
What is the TEMPEST ELECTRIC WHEELCHAIR?
TEMPEST ELECTRIC WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K904958.
When did TEMPEST ELECTRIC WHEELCHAIR receive FDA 510(k) clearance?
TEMPEST ELECTRIC WHEELCHAIR received FDA 510(k) clearance on 1990-11-26, under 510(k) number K904958.
Who is the listed applicant for TEMPEST ELECTRIC 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 TEMPEST ELECTRIC WHEELCHAIR?
The FDA product code for TEMPEST ELECTRIC WHEELCHAIR is ITI.
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: ITI)
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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