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FDA 510(k)

NEURAL STIMULATOR MONITOR

K-Number: K833809 · 1983-12-01

ApplicantInstromedix, Inc.
Decision Date1983-12-01
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURAL STIMULATOR MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Instromedix, Inc.. It received FDA 510(k) clearance on 1983-12-01 under 510(k) number K833809. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURAL STIMULATOR MONITOR?

NEURAL STIMULATOR MONITOR is a medical device that received FDA 510(k) clearance on 1983-12-01. The listed applicant is Instromedix, Inc.. The 510(k) number is K833809.

When did NEURAL STIMULATOR MONITOR receive FDA 510(k) clearance?

NEURAL STIMULATOR MONITOR received FDA 510(k) clearance on 1983-12-01, under 510(k) number K833809.

Who is the listed applicant for NEURAL STIMULATOR MONITOR?

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

What is the FDA product code for NEURAL STIMULATOR MONITOR?

The FDA product code for NEURAL STIMULATOR MONITOR is GZB.

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Related Devices (Code: GZB)

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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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