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FDA 510(k)

KNEE-HIP MOBILIZER

K-Number: K842881 · 1984-08-08

ApplicantJoint Mobilizer Systems, Inc.
Decision Date1984-08-08
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KNEE-HIP MOBILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Joint Mobilizer Systems, Inc.. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K842881. 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 KNEE-HIP MOBILIZER?

KNEE-HIP MOBILIZER is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Joint Mobilizer Systems, Inc.. The 510(k) number is K842881.

When did KNEE-HIP MOBILIZER receive FDA 510(k) clearance?

KNEE-HIP MOBILIZER received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842881.

Who is the listed applicant for KNEE-HIP MOBILIZER?

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

What is the FDA product code for KNEE-HIP MOBILIZER?

The FDA product code for KNEE-HIP MOBILIZER 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 Joint Mobilizer Systems, 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.

K842882ANKLE MOBILIZER

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.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment 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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