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FDA 510(k)

CNS-EP SYSTEM AND EP 1.0 SOFTWARE

K-Number: K860240 · 1986-04-17

ApplicantCns, Inc.
Decision Date1986-04-17
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CNS-EP SYSTEM AND EP 1.0 SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Cns, Inc.. It received FDA 510(k) clearance on 1986-04-17 under 510(k) number K860240. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CNS-EP SYSTEM AND EP 1.0 SOFTWARE?

CNS-EP SYSTEM AND EP 1.0 SOFTWARE is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Cns, Inc.. The 510(k) number is K860240.

When did CNS-EP SYSTEM AND EP 1.0 SOFTWARE receive FDA 510(k) clearance?

CNS-EP SYSTEM AND EP 1.0 SOFTWARE received FDA 510(k) clearance on 1986-04-17, under 510(k) number K860240.

Who is the listed applicant for CNS-EP SYSTEM AND EP 1.0 SOFTWARE?

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

What is the FDA product code for CNS-EP SYSTEM AND EP 1.0 SOFTWARE?

The FDA product code for CNS-EP SYSTEM AND EP 1.0 SOFTWARE is GWF.

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Other records listing Cns, Inc. as applicant

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Related Devices (Code: GWF)

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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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