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FDA 510(k)

STIMULATOR, NIC-106 VISUAL

K-Number: K790570 · 1979-05-23

ApplicantNicolet Biomedical Instruments
Decision Date1979-05-23
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, NIC-106 VISUAL is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical Instruments. It received FDA 510(k) clearance on 1979-05-23 under 510(k) number K790570. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, NIC-106 VISUAL?

STIMULATOR, NIC-106 VISUAL is a medical device that received FDA 510(k) clearance on 1979-05-23. The listed applicant is Nicolet Biomedical Instruments. The 510(k) number is K790570.

When did STIMULATOR, NIC-106 VISUAL receive FDA 510(k) clearance?

STIMULATOR, NIC-106 VISUAL received FDA 510(k) clearance on 1979-05-23, under 510(k) number K790570.

Who is the listed applicant for STIMULATOR, NIC-106 VISUAL?

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

What is the FDA product code for STIMULATOR, NIC-106 VISUAL?

The FDA product code for STIMULATOR, NIC-106 VISUAL is GWE.

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Other records listing Nicolet Biomedical Instruments as applicant

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.

K880573MODIFIED NICOLET VIKING SYSTEMK873736NICOLET DIGITAL TWO PIECE HEARING AIDK873964NICOLET DISPOSABLE PRASS PROBEK873535NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEMK871678NICOLET AMP 6R11 SYSTEMK862592PHOENIX SYSTEM SEVEN.

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Related Devices (Code: GWE)

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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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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