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FDA 510(k)

FMA TRANSLATOR

K-Number: K912086 · 1991-08-07

ApplicantNormandie Group, Inc.
Decision Date1991-08-07
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FMA TRANSLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Normandie Group, Inc.. It received FDA 510(k) clearance on 1991-08-07 under 510(k) number K912086. 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 FMA TRANSLATOR?

FMA TRANSLATOR is a medical device that received FDA 510(k) clearance on 1991-08-07. The listed applicant is Normandie Group, Inc.. The 510(k) number is K912086.

When did FMA TRANSLATOR receive FDA 510(k) clearance?

FMA TRANSLATOR received FDA 510(k) clearance on 1991-08-07, under 510(k) number K912086.

Who is the listed applicant for FMA TRANSLATOR?

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

What is the FDA product code for FMA TRANSLATOR?

The FDA product code for FMA TRANSLATOR is BXB.

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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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