FDA 510(k)

CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON

K-Number: K926424 · 1993-11-19

Decision Date1993-11-19

Product CodeGYC

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K926424. The device is classified under product code GYC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON?

CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Radionics, Inc.. The 510(k) number is K926424.

When did CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON receive FDA 510(k) clearance?

CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON received FDA 510(k) clearance on 1993-11-19, under 510(k) number K926424.

Who is the listed applicant for CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON?

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

What is the FDA product code for CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON?

The FDA product code for CORTICAL SURF EPILEPSY ELECT DEPTH ELEC EPILEP MON is GYC.

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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.