ARM THROUGH FOR WHEELCHAIR BK 6454-01 &
K-Number: K823638 · 1983-01-21
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Device Summary
Frequently Asked Questions
What is the ARM THROUGH FOR WHEELCHAIR BK 6454-01 &?
ARM THROUGH FOR WHEELCHAIR BK 6454-01 & is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K823638.
When did ARM THROUGH FOR WHEELCHAIR BK 6454-01 & receive FDA 510(k) clearance?
ARM THROUGH FOR WHEELCHAIR BK 6454-01 & received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823638.
Who is the listed applicant for ARM THROUGH FOR WHEELCHAIR BK 6454-01 &?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARM THROUGH FOR WHEELCHAIR BK 6454-01 &?
The FDA product code for ARM THROUGH FOR WHEELCHAIR BK 6454-01 & 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 Fred Sammons, 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: 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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