BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF
K-Number: K801709 · 1980-08-07
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Device Summary
Frequently Asked Questions
What is the BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF?
BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K801709.
When did BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF receive FDA 510(k) clearance?
BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801709.
Who is the listed applicant for BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF?
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 BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF?
The FDA product code for BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF 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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