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FDA 510(k)

A.C. POWER PATIENT LIFT

K-Number: K935351 · 1994-02-28

ApplicantKen Kemmerer
Decision Date1994-02-28
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A.C. POWER PATIENT LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Ken Kemmerer. It received FDA 510(k) clearance on 1994-02-28 under 510(k) number K935351. 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 A.C. POWER PATIENT LIFT?

A.C. POWER PATIENT LIFT is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Ken Kemmerer. The 510(k) number is K935351.

When did A.C. POWER PATIENT LIFT receive FDA 510(k) clearance?

A.C. POWER PATIENT LIFT received FDA 510(k) clearance on 1994-02-28, under 510(k) number K935351.

Who is the listed applicant for A.C. POWER PATIENT LIFT?

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

What is the FDA product code for A.C. POWER PATIENT LIFT?

The FDA product code for A.C. POWER PATIENT LIFT 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ken Kemmerer 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.

K961663ELECTRIC SEAT LIFT CHAIR

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.K926411SAF-LIFT/SAF-KARYArjo-Century, Inc.K912769PATIENT LIFT AND TRANSPORTCentury Manufacturing Co.K905414MANGAR BOOSTERNorthfleet Management Group, Inc.

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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