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FDA 510(k)

INSTA-NERVE(TM) NERVE CONDUCTION MONITOR

K-Number: K935298 · 1994-08-03

ApplicantInsta Nerve Canada, Inc.
Decision Date1994-08-03
Product CodeJXE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INSTA-NERVE(TM) NERVE CONDUCTION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Insta Nerve Canada, Inc.. It received FDA 510(k) clearance on 1994-08-03 under 510(k) number K935298. The device is classified under product code JXE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTA-NERVE(TM) NERVE CONDUCTION MONITOR?

INSTA-NERVE(TM) NERVE CONDUCTION MONITOR is a medical device that received FDA 510(k) clearance on 1994-08-03. The listed applicant is Insta Nerve Canada, Inc.. The 510(k) number is K935298.

When did INSTA-NERVE(TM) NERVE CONDUCTION MONITOR receive FDA 510(k) clearance?

INSTA-NERVE(TM) NERVE CONDUCTION MONITOR received FDA 510(k) clearance on 1994-08-03, under 510(k) number K935298.

Who is the listed applicant for INSTA-NERVE(TM) NERVE CONDUCTION MONITOR?

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

What is the FDA product code for INSTA-NERVE(TM) NERVE CONDUCTION MONITOR?

The FDA product code for INSTA-NERVE(TM) NERVE CONDUCTION MONITOR is JXE.

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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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