FDA 510(k)

GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS

K-Number: K943896 · 1995-12-22

Decision Date1995-12-22

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1995-12-22 under 510(k) number K943896. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS?

GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Datascope Corp.. The 510(k) number is K943896.

When did GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS receive FDA 510(k) clearance?

GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS received FDA 510(k) clearance on 1995-12-22, under 510(k) number K943896.

Who is the listed applicant for GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS?

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

What is the FDA product code for GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS?

The FDA product code for GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS is DQX.

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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.