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FDA 510(k)

PERSONAL TRANSFER SYSTEM

K-Number: K885270 · 1989-03-14

ApplicantColumbus Mckinnon Corp.
Decision Date1989-03-14
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERSONAL TRANSFER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Columbus Mckinnon Corp.. It received FDA 510(k) clearance on 1989-03-14 under 510(k) number K885270. 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 PERSONAL TRANSFER SYSTEM?

PERSONAL TRANSFER SYSTEM is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is Columbus Mckinnon Corp.. The 510(k) number is K885270.

When did PERSONAL TRANSFER SYSTEM receive FDA 510(k) clearance?

PERSONAL TRANSFER SYSTEM received FDA 510(k) clearance on 1989-03-14, under 510(k) number K885270.

Who is the listed applicant for PERSONAL TRANSFER SYSTEM?

The FDA 510(k) record lists Columbus Mckinnon Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERSONAL TRANSFER SYSTEM?

The FDA product code for PERSONAL TRANSFER SYSTEM 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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