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FDA 510(k)

LATERAL FLEXION MACHINE

K-Number: K940455 · 1995-01-12

ApplicantRehab, Inc.
Decision Date1995-01-12
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

LATERAL FLEXION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Rehab, Inc.. It received FDA 510(k) clearance on 1995-01-12 under 510(k) number K940455. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the LATERAL FLEXION MACHINE?

LATERAL FLEXION MACHINE is a medical device that received FDA 510(k) clearance on 1995-01-12. The listed applicant is Rehab, Inc.. The 510(k) number is K940455.

When did LATERAL FLEXION MACHINE receive FDA 510(k) clearance?

LATERAL FLEXION MACHINE received FDA 510(k) clearance on 1995-01-12, under 510(k) number K940455.

Who is the listed applicant for LATERAL FLEXION MACHINE?

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

What is the FDA product code for LATERAL FLEXION MACHINE?

The FDA product code for LATERAL FLEXION MACHINE is BXB.

Related Clinical Trials

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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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