FDA 510(k)

MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER

K-Number: K914479 · 1994-03-07

Decision Date1994-03-07

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER 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 1994-03-07 under 510(k) number K914479. 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 MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER?

MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K914479.

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

MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER received FDA 510(k) clearance on 1994-03-07, under 510(k) number K914479.

Who is the listed applicant for MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER?

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 MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER?

The FDA product code for MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCER 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.