FDA 510(k)

INTRACRANIAL PRESSURE MONITORING

K-Number: K790920 · 1979-08-03

Decision Date1979-08-03

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

INTRACRANIAL PRESSURE MONITORING is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K790920. 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 INTRACRANIAL PRESSURE MONITORING?

INTRACRANIAL PRESSURE MONITORING is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K790920.

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

INTRACRANIAL PRESSURE MONITORING received FDA 510(k) clearance on 1979-08-03, under 510(k) number K790920.

Who is the listed applicant for INTRACRANIAL PRESSURE MONITORING?

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

What is the FDA product code for INTRACRANIAL PRESSURE MONITORING?

The FDA product code for INTRACRANIAL PRESSURE MONITORING is 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.