FDA 510(k)

SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE

K-Number: K864320 · 1987-02-20

Decision Date1987-02-20

Product CodeDRQ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K864320. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE?

SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Cordis Corp.. The 510(k) number is K864320.

When did SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE receive FDA 510(k) clearance?

SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE received FDA 510(k) clearance on 1987-02-20, under 510(k) number K864320.

Who is the listed applicant for SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE?

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 SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE?

The FDA product code for SENTRON PRESSURE MEASURING CATH/PRESSURE INTERFACE is DRQ.

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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.