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FDA 510(k)

TAYLOR PATIENT TRANSFER BOARD

K-Number: K792247 · 1979-11-30

Decision Date1979-11-30
Product CodeIKX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TAYLOR PATIENT TRANSFER BOARD is the device name listed in this FDA 510(k) record. The listed applicant is Taylor Medical Equipment. It received FDA 510(k) clearance on 1979-11-30 under 510(k) number K792247. The device is classified under product code IKX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAYLOR PATIENT TRANSFER BOARD?

TAYLOR PATIENT TRANSFER BOARD is a medical device that received FDA 510(k) clearance on 1979-11-30. The listed applicant is Taylor Medical Equipment. The 510(k) number is K792247.

When did TAYLOR PATIENT TRANSFER BOARD receive FDA 510(k) clearance?

TAYLOR PATIENT TRANSFER BOARD received FDA 510(k) clearance on 1979-11-30, under 510(k) number K792247.

Who is the listed applicant for TAYLOR PATIENT TRANSFER BOARD?

The FDA 510(k) record lists Taylor Medical Equipment as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAYLOR PATIENT TRANSFER BOARD?

The FDA product code for TAYLOR PATIENT TRANSFER BOARD is IKX.

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 Taylor Medical Equipment 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: IKX)

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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