FDA 510(k)

CEREBRAL FUNCTION MONITOR 870

K-Number: K791580 · 1979-09-04

Decision Date1979-09-04

Product CodeOMA

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CEREBRAL FUNCTION MONITOR 870 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Research. It received FDA 510(k) clearance on 1979-09-04 under 510(k) number K791580. The device is classified under product code OMA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREBRAL FUNCTION MONITOR 870?

CEREBRAL FUNCTION MONITOR 870 is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Applied Medical Research. The 510(k) number is K791580.

When did CEREBRAL FUNCTION MONITOR 870 receive FDA 510(k) clearance?

CEREBRAL FUNCTION MONITOR 870 received FDA 510(k) clearance on 1979-09-04, under 510(k) number K791580.

Who is the listed applicant for CEREBRAL FUNCTION MONITOR 870?

The FDA 510(k) record lists Applied Medical Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEREBRAL FUNCTION MONITOR 870?

The FDA product code for CEREBRAL FUNCTION MONITOR 870 is OMA.

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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.