FDA 510(k)

METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM

K-Number: K880154 · 1988-03-28

Decision Date1988-03-28

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Metatech Corp.. It received FDA 510(k) clearance on 1988-03-28 under 510(k) number K880154. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM?

METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-28. The listed applicant is Metatech Corp.. The 510(k) number is K880154.

When did METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?

METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 1988-03-28, under 510(k) number K880154.

Who is the listed applicant for METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM?

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

What is the FDA product code for METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM?

The FDA product code for METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM is GWM.

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Related Devices (Code: GWM)

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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.