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FDA 510(k)

CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD

K-Number: K871012 · 1987-03-25

ApplicantCropper Medical, Inc.
Decision Date1987-03-25
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD is the device name listed in this FDA 510(k) record. The listed applicant is Cropper Medical, Inc.. It received FDA 510(k) clearance on 1987-03-25 under 510(k) number K871012. 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 CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD?

CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD is a medical device that received FDA 510(k) clearance on 1987-03-25. The listed applicant is Cropper Medical, Inc.. The 510(k) number is K871012.

When did CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD receive FDA 510(k) clearance?

CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD received FDA 510(k) clearance on 1987-03-25, under 510(k) number K871012.

Who is the listed applicant for CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD?

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

What is the FDA product code for CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD?

The FDA product code for CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD 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 Cropper Medical, 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.

K844995SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE

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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