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FDA 510(k)

CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS

K-Number: K853420 · 1986-02-07

ApplicantAlvar
Decision Date1986-02-07
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS is the device name listed in this FDA 510(k) record. The listed applicant is Alvar. It received FDA 510(k) clearance on 1986-02-07 under 510(k) number K853420. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS?

CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Alvar. The 510(k) number is K853420.

When did CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS receive FDA 510(k) clearance?

CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS received FDA 510(k) clearance on 1986-02-07, under 510(k) number K853420.

Who is the listed applicant for CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS?

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

What is the FDA product code for CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS?

The FDA product code for CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS is OLT.

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Related Devices (Code: OLT)

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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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