ADJUSTER, WHEELCHAIR WIDTH, BK-6470
K-Number: K760296 · 1976-09-08
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Device Summary
Frequently Asked Questions
What is the ADJUSTER, WHEELCHAIR WIDTH, BK-6470?
ADJUSTER, WHEELCHAIR WIDTH, BK-6470 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760296.
When did ADJUSTER, WHEELCHAIR WIDTH, BK-6470 receive FDA 510(k) clearance?
ADJUSTER, WHEELCHAIR WIDTH, BK-6470 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760296.
Who is the listed applicant for ADJUSTER, WHEELCHAIR WIDTH, BK-6470?
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 ADJUSTER, WHEELCHAIR WIDTH, BK-6470?
The FDA product code for ADJUSTER, WHEELCHAIR WIDTH, BK-6470 is KNO.
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: KNO)
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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