FDA 510(k)

E-Z FLEX

K-Number: K953456 · 1996-01-26

ApplicantFluid Motion Biotechnologies, Inc.

Decision Date1996-01-26

Product CodeBXB

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

E-Z FLEX is the device name listed in this FDA 510(k) record. The listed applicant is Fluid Motion Biotechnologies, Inc.. It received FDA 510(k) clearance on 1996-01-26 under 510(k) number K953456. 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 E-Z FLEX?

E-Z FLEX is a medical device that received FDA 510(k) clearance on 1996-01-26. The listed applicant is Fluid Motion Biotechnologies, Inc.. The 510(k) number is K953456.

When did E-Z FLEX receive FDA 510(k) clearance?

E-Z FLEX received FDA 510(k) clearance on 1996-01-26, under 510(k) number K953456.

Who is the listed applicant for E-Z FLEX?

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

What is the FDA product code for E-Z FLEX?

The FDA product code for E-Z FLEX is BXB.

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, LLC K952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K951028HAMEX TWONorthern Orthopaedic Products, Inc.

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.