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FDA 510(k)

MEUROMETRICS MONITOR

K-Number: K803233 · 1981-01-12

ApplicantDade Medical, Inc.
Decision Date1981-01-12
Product CodeGWS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEUROMETRICS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Dade Medical, Inc.. It received FDA 510(k) clearance on 1981-01-12 under 510(k) number K803233. The device is classified under product code GWS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEUROMETRICS MONITOR?

MEUROMETRICS MONITOR is a medical device that received FDA 510(k) clearance on 1981-01-12. The listed applicant is Dade Medical, Inc.. The 510(k) number is K803233.

When did MEUROMETRICS MONITOR receive FDA 510(k) clearance?

MEUROMETRICS MONITOR received FDA 510(k) clearance on 1981-01-12, under 510(k) number K803233.

Who is the listed applicant for MEUROMETRICS MONITOR?

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

What is the FDA product code for MEUROMETRICS MONITOR?

The FDA product code for MEUROMETRICS MONITOR is GWS.

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Related Devices (Code: GWS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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