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FDA 510(k)

BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF

K-Number: K801709 · 1980-08-07

Decision Date1980-08-07
Product CodeKNO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BK-5058-01 QUAD-QUIP WHEELCHAIR CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1980-08-07 under 510(k) number K801709. The device is classified under product code KNO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 278 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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