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FDA 510(k)

TST - SUPPRESSOR MODEL #1000

K-Number: K013827 · 2002-05-21

ApplicantNeurosim Limited
Decision Date2002-05-21
Product CodeKLW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TST - SUPPRESSOR MODEL #1000 is the device name listed in this FDA 510(k) record. The listed applicant is Neurosim Limited. It received FDA 510(k) clearance on 2002-05-21 under 510(k) number K013827. The device is classified under product code KLW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TST - SUPPRESSOR MODEL #1000?

TST - SUPPRESSOR MODEL #1000 is a medical device that received FDA 510(k) clearance on 2002-05-21. The listed applicant is Neurosim Limited. The 510(k) number is K013827.

When did TST - SUPPRESSOR MODEL #1000 receive FDA 510(k) clearance?

TST - SUPPRESSOR MODEL #1000 received FDA 510(k) clearance on 2002-05-21, under 510(k) number K013827.

Who is the listed applicant for TST - SUPPRESSOR MODEL #1000?

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

What is the FDA product code for TST - SUPPRESSOR MODEL #1000?

The FDA product code for TST - SUPPRESSOR MODEL #1000 is KLW.

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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.

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