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FDA 510(k)

CONTROLLED PASSIVE MOTION MACHINE

K-Number: K920860 · 1992-04-02

ApplicantU.S. Mfg. & Management, Inc.
Decision Date1992-04-02
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTROLLED PASSIVE MOTION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Mfg. & Management, Inc.. It received FDA 510(k) clearance on 1992-04-02 under 510(k) number K920860. 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 CONTROLLED PASSIVE MOTION MACHINE?

CONTROLLED PASSIVE MOTION MACHINE is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is U.S. Mfg. & Management, Inc.. The 510(k) number is K920860.

When did CONTROLLED PASSIVE MOTION MACHINE receive FDA 510(k) clearance?

CONTROLLED PASSIVE MOTION MACHINE received FDA 510(k) clearance on 1992-04-02, under 510(k) number K920860.

Who is the listed applicant for CONTROLLED PASSIVE MOTION MACHINE?

The FDA 510(k) record lists U.S. Mfg. & Management, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTROLLED PASSIVE MOTION MACHINE?

The FDA product code for CONTROLLED PASSIVE MOTION MACHINE 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 U.S. Mfg. & Management, 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.

K874436FLUID SAMPLING PACKK862335MODIFIED I.V. START, RE-START, PEDI AND GERI-KITK853242I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KIK842999VENI-SHIELD

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

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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