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FDA 510(k)

LIFT MASTER PATIENT LIFT

K-Number: K896848 · 1990-05-29

ApplicantHenry Enterprises, Inc.
Decision Date1990-05-29
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFT MASTER PATIENT LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Henry Enterprises, Inc.. It received FDA 510(k) clearance on 1990-05-29 under 510(k) number K896848. 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 LIFT MASTER PATIENT LIFT?

LIFT MASTER PATIENT LIFT is a medical device that received FDA 510(k) clearance on 1990-05-29. The listed applicant is Henry Enterprises, Inc.. The 510(k) number is K896848.

When did LIFT MASTER PATIENT LIFT receive FDA 510(k) clearance?

LIFT MASTER PATIENT LIFT received FDA 510(k) clearance on 1990-05-29, under 510(k) number K896848.

Who is the listed applicant for LIFT MASTER PATIENT LIFT?

The FDA 510(k) record lists Henry Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFT MASTER PATIENT LIFT?

The FDA product code for LIFT MASTER PATIENT LIFT is FNG.

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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

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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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