BERKELEY BRAKE
K-Number: K823874 · 1983-01-14
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Device Summary
Frequently Asked Questions
What is the BERKELEY BRAKE?
BERKELEY BRAKE is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Berkeley Electric Wheelchair Co.. The 510(k) number is K823874.
When did BERKELEY BRAKE receive FDA 510(k) clearance?
BERKELEY BRAKE received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823874.
Who is the listed applicant for BERKELEY BRAKE?
The FDA 510(k) record lists Berkeley Electric Wheelchair Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BERKELEY BRAKE?
The FDA product code for BERKELEY BRAKE is KNN.
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 Berkeley Electric Wheelchair Co. 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: KNN)
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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