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FDA 510(k)

CERVICAL PASSIVE MOTION

K-Number: K921323 · 1992-06-03

ApplicantRehabilitative Resources, Inc.
Decision Date1992-06-03
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERVICAL PASSIVE MOTION 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 1992-06-03 under 510(k) number K921323. 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 CERVICAL PASSIVE MOTION?

CERVICAL PASSIVE MOTION is a medical device that received FDA 510(k) clearance on 1992-06-03. The listed applicant is Rehabilitative Resources, Inc.. The 510(k) number is K921323.

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

CERVICAL PASSIVE MOTION received FDA 510(k) clearance on 1992-06-03, under 510(k) number K921323.

Who is the listed applicant for CERVICAL PASSIVE MOTION?

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 CERVICAL PASSIVE MOTION?

The FDA product code for CERVICAL PASSIVE MOTION 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.

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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.

K920519LUMBAR CPM

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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