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FDA 510(k)

DRUALIFT 500

K-Number: K801933 · 1980-08-27

ApplicantIndependent Transfer Equipment Co.
Decision Date1980-08-27
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DRUALIFT 500 is the device name listed in this FDA 510(k) record. The listed applicant is Independent Transfer Equipment Co.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801933. The device is classified under product code FNG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRUALIFT 500?

DRUALIFT 500 is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Independent Transfer Equipment Co.. The 510(k) number is K801933.

When did DRUALIFT 500 receive FDA 510(k) clearance?

DRUALIFT 500 received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801933.

Who is the listed applicant for DRUALIFT 500?

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

What is the FDA product code for DRUALIFT 500?

The FDA product code for DRUALIFT 500 is FNG.

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.

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Other records listing Independent Transfer Equipment 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.

K803063STRAP EASE 400

Related Devices (Code: FNG)

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.

K121287HT-WEDGED.T. Davis Enterprises Ltd. T/A Hovertech Int'LK041503HOVERJACK AIR PATIENT LIFT DEVICED.T. Davis Enterprises , Ltd.K940872PATIENT SUPPORT SYSTEMArylift, Inc.K935351A.C. POWER PATIENT LIFTKen KemmererK926411SAF-LIFT/SAF-KARYArjo-Century, Inc.K912769PATIENT LIFT AND TRANSPORTCentury Manufacturing Co.

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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