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FDA 510(k)

CONTINUOUS PASSIVE MOTION

K-Number: K841674 · 1984-05-09

ApplicantChattanooga Group, Inc.
Decision Date1984-05-09
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS PASSIVE MOTION is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841674. 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?

CONTINUOUS PASSIVE MOTION is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K841674.

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

CONTINUOUS PASSIVE MOTION received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841674.

Who is the listed applicant for CONTINUOUS PASSIVE MOTION?

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

What is the FDA product code for CONTINUOUS PASSIVE MOTION?

The FDA product code for CONTINUOUS PASSIVE MOTION is BXB.

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Other records listing Chattanooga Group, 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.

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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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