FDA 510(k)

CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER

K-Number: K940648 · 1995-03-01

Decision Date1995-03-01

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1995-03-01 under 510(k) number K940648. 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 CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER?

CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Cordis Corp.. The 510(k) number is K940648.

When did CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER receive FDA 510(k) clearance?

CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER received FDA 510(k) clearance on 1995-03-01, under 510(k) number K940648.

Who is the listed applicant for CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER?

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

What is the FDA product code for CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER?

The FDA product code for CORDIS DISPOSABLE ICP 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.