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FDA 510(k)

NERVE MONITOR ELECTRODES/STIMULATOR PROBES

K-Number: K945242 · 1994-12-27

ApplicantMicromed Development Corp.
Decision Date1994-12-27
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NERVE MONITOR ELECTRODES/STIMULATOR PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Micromed Development Corp.. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K945242. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NERVE MONITOR ELECTRODES/STIMULATOR PROBES?

NERVE MONITOR ELECTRODES/STIMULATOR PROBES is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Micromed Development Corp.. The 510(k) number is K945242.

When did NERVE MONITOR ELECTRODES/STIMULATOR PROBES receive FDA 510(k) clearance?

NERVE MONITOR ELECTRODES/STIMULATOR PROBES received FDA 510(k) clearance on 1994-12-27, under 510(k) number K945242.

Who is the listed applicant for NERVE MONITOR ELECTRODES/STIMULATOR PROBES?

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

What is the FDA product code for NERVE MONITOR ELECTRODES/STIMULATOR PROBES?

The FDA product code for NERVE MONITOR ELECTRODES/STIMULATOR PROBES is ETN.

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Other records listing Micromed Development Corp. 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.

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Related Devices (Code: ETN)

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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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