FDA 510(k)

TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP

K-Number: K020780 · 2002-05-20

Decision Date2002-05-20

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 2002-05-20 under 510(k) number K020780. 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 TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP?

TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP is a medical device that received FDA 510(k) clearance on 2002-05-20. The listed applicant is Medex, Inc.. The 510(k) number is K020780.

When did TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP receive FDA 510(k) clearance?

TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP received FDA 510(k) clearance on 2002-05-20, under 510(k) number K020780.

Who is the listed applicant for TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP?

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

What is the FDA product code for TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP?

The FDA product code for TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP is GWM.

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Related Devices (Code: GWM)

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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.