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FDA 510(k)

MURRAY CHAIR LIFT

K-Number: K854120 · 1985-11-01

ApplicantJ.B. Murray Enterprises, Inc.
Decision Date1985-11-01
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MURRAY CHAIR LIFT is the device name listed in this FDA 510(k) record. The listed applicant is J.B. Murray Enterprises, Inc.. It received FDA 510(k) clearance on 1985-11-01 under 510(k) number K854120. 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 MURRAY CHAIR LIFT?

MURRAY CHAIR LIFT is a medical device that received FDA 510(k) clearance on 1985-11-01. The listed applicant is J.B. Murray Enterprises, Inc.. The 510(k) number is K854120.

When did MURRAY CHAIR LIFT receive FDA 510(k) clearance?

MURRAY CHAIR LIFT received FDA 510(k) clearance on 1985-11-01, under 510(k) number K854120.

Who is the listed applicant for MURRAY CHAIR LIFT?

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

What is the FDA product code for MURRAY CHAIR LIFT?

The FDA product code for MURRAY CHAIR 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

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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