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FDA 510(k)

PATIENT MOVER(TM)

K-Number: K890555 · 1989-02-13

ApplicantT.B.S., Inc.
Decision Date1989-02-13
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PATIENT MOVER(TM) is the device name listed in this FDA 510(k) record. The listed applicant is T.B.S., Inc.. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K890555. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MOVER(TM)?

PATIENT MOVER(TM) is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is T.B.S., Inc.. The 510(k) number is K890555.

When did PATIENT MOVER(TM) receive FDA 510(k) clearance?

PATIENT MOVER(TM) received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890555.

Who is the listed applicant for PATIENT MOVER(TM)?

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

What is the FDA product code for PATIENT MOVER(TM)?

The FDA product code for PATIENT MOVER(TM) is ILK.

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 T.B.S., Inc. 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.

K871582PATIENT MOVER(TM)

Related Devices (Code: ILK)

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.

K240843GENESIS (MS-P02-GEN)Climbing Steps, Inc.K222818Xpedition ™ Powered Stair Chair (625700000000)Stryker MedicalK121560LEVANT, HOMEGLIDEThyssenkrupp Accessibility B.V.K121561FLOW2, SWINGThyssenkrupp Accessibility B.V.K113308BRUNO ELAN STAIRWAY ELEVATORBruno Independent Living Aids, Inc.K111858LIFTKAR PTSano Transportgeraete GmbH

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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