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FDA 510(k)

KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE

K-Number: K952369 · 1995-08-07

ApplicantPhysicians Consulting, Inc.
Decision Date1995-08-07
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Physicians Consulting, Inc.. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K952369. 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 KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE?

KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Physicians Consulting, Inc.. The 510(k) number is K952369.

When did KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE receive FDA 510(k) clearance?

KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE received FDA 510(k) clearance on 1995-08-07, under 510(k) number K952369.

Who is the listed applicant for KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE?

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

What is the FDA product code for KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE?

The FDA product code for KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE 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 Physicians Consulting, 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.

K944819KRDL 2000

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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