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FDA 510(k)

PARAMED LATERAL FLEXION MACHINE

K-Number: K923494 · 1992-11-09

ApplicantParamed Div
Decision Date1992-11-09
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PARAMED LATERAL FLEXION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Paramed Div. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K923494. 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 PARAMED LATERAL FLEXION MACHINE?

PARAMED LATERAL FLEXION MACHINE is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Paramed Div. The 510(k) number is K923494.

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

PARAMED LATERAL FLEXION MACHINE received FDA 510(k) clearance on 1992-11-09, under 510(k) number K923494.

Who is the listed applicant for PARAMED LATERAL FLEXION MACHINE?

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

What is the FDA product code for PARAMED LATERAL FLEXION MACHINE?

The FDA product code for PARAMED LATERAL FLEXION 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.

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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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