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FDA 510(k)

BED TRAY

K-Number: K761110 · 1976-12-02

Decision Date1976-12-02
Product CodeKMN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED TRAY 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 1976-12-02 under 510(k) number K761110. The device is classified under product code KMN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BED TRAY?

BED TRAY is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K761110.

When did BED TRAY receive FDA 510(k) clearance?

BED TRAY received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761110.

Who is the listed applicant for BED TRAY?

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 BED TRAY?

The FDA product code for BED TRAY is KMN.

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: KMN)

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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