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FDA 510(k)

LUMBAR CPM

K-Number: K920519 · 1992-03-13

ApplicantRehabilitative Resources, Inc.
Decision Date1992-03-13
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LUMBAR CPM is the device name listed in this FDA 510(k) record. The listed applicant is Rehabilitative Resources, Inc.. It received FDA 510(k) clearance on 1992-03-13 under 510(k) number K920519. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMBAR CPM?

LUMBAR CPM is a medical device that received FDA 510(k) clearance on 1992-03-13. The listed applicant is Rehabilitative Resources, Inc.. The 510(k) number is K920519.

When did LUMBAR CPM receive FDA 510(k) clearance?

LUMBAR CPM received FDA 510(k) clearance on 1992-03-13, under 510(k) number K920519.

Who is the listed applicant for LUMBAR CPM?

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

What is the FDA product code for LUMBAR CPM?

The FDA product code for LUMBAR CPM is BXB.

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 Rehabilitative Resources, 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.

K921323CERVICAL PASSIVE MOTION

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment 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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