FDA 510(k)

NTI-1000

K-Number: K894097 · 1989-09-25

Decision Date1989-09-25

Product CodeQJQ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NTI-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Neurotek, Inc.. It received FDA 510(k) clearance on 1989-09-25 under 510(k) number K894097. The device is classified under product code QJQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NTI-1000?

NTI-1000 is a medical device that received FDA 510(k) clearance on 1989-09-25. The listed applicant is Neurotek, Inc.. The 510(k) number is K894097.

When did NTI-1000 receive FDA 510(k) clearance?

NTI-1000 received FDA 510(k) clearance on 1989-09-25, under 510(k) number K894097.

Who is the listed applicant for NTI-1000?

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

What is the FDA product code for NTI-1000?

The FDA product code for NTI-1000 is QJQ.

Related Devices (Code: QJQ)

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.

K252951Genesis SleepNeurofield, Inc.K232253Modius StressNeurovalens Limited K230826Modius SleepNeurovalens , Ltd.K182311CervellaInnovative Neurological Devices, LLC K090052CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/CJohari Digital Healthcare , Ltd.K070412ELEXOMA MEDICRedplane AG

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.