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FDA 510(k)

DESK ARM WHEELCHAIR ARM EXTENSION

K-Number: K812348 · 1981-09-11

Decision Date1981-09-11
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DESK ARM WHEELCHAIR ARM EXTENSION 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 1981-09-11 under 510(k) number K812348. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESK ARM WHEELCHAIR ARM EXTENSION?

DESK ARM WHEELCHAIR ARM EXTENSION is a medical device that received FDA 510(k) clearance on 1981-09-11. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K812348.

When did DESK ARM WHEELCHAIR ARM EXTENSION receive FDA 510(k) clearance?

DESK ARM WHEELCHAIR ARM EXTENSION received FDA 510(k) clearance on 1981-09-11, under 510(k) number K812348.

Who is the listed applicant for DESK ARM WHEELCHAIR ARM EXTENSION?

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 DESK ARM WHEELCHAIR ARM EXTENSION?

The FDA product code for DESK ARM WHEELCHAIR ARM EXTENSION 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.

View all 278 devices →

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

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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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