FDA 510(k)

ELECTRODE FOR NEUROLOGICAL SURGERY 2111

K-Number: K845035 · 1985-07-30

Decision Date1985-07-30

Product CodeGYC

Advisory CommitteeNE

DecisionSubstantially Equivalent for Some Indications

Device Summary

ELECTRODE FOR NEUROLOGICAL SURGERY 2111 is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1985-07-30 under 510(k) number K845035. The device is classified under product code GYC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ELECTRODE FOR NEUROLOGICAL SURGERY 2111?

ELECTRODE FOR NEUROLOGICAL SURGERY 2111 is a medical device that received FDA 510(k) clearance on 1985-07-30. The listed applicant is Progress Mankind Technology. The 510(k) number is K845035.

When did ELECTRODE FOR NEUROLOGICAL SURGERY 2111 receive FDA 510(k) clearance?

ELECTRODE FOR NEUROLOGICAL SURGERY 2111 received FDA 510(k) clearance on 1985-07-30, under 510(k) number K845035.

Who is the listed applicant for ELECTRODE FOR NEUROLOGICAL SURGERY 2111?

The FDA 510(k) record lists Progress Mankind Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRODE FOR NEUROLOGICAL SURGERY 2111?

The FDA product code for ELECTRODE FOR NEUROLOGICAL SURGERY 2111 is GYC.

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Related Devices (Code: 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.