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FDA 510(k)

POSEY BED

K-Number: K113355 · 2012-05-02

Decision Date2012-05-02
Product CodeOYS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POSEY BED is the device name listed in this FDA 510(k) record. The listed applicant is J. T. Posey Co.. It received FDA 510(k) clearance on 2012-05-02 under 510(k) number K113355. The device is classified under product code OYS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSEY BED?

POSEY BED is a medical device that received FDA 510(k) clearance on 2012-05-02. The listed applicant is J. T. Posey Co.. The 510(k) number is K113355.

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

POSEY BED received FDA 510(k) clearance on 2012-05-02, under 510(k) number K113355.

Who is the listed applicant for POSEY BED?

The FDA 510(k) record lists J. T. Posey Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSEY BED?

The FDA product code for POSEY BED is OYS.

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 J. T. Posey Co. 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 13 devices →

Related Devices (Code: OYS)

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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