FDA 510(k)

INTERVENTIONAL PRODUCTS - GUIDE WIRES

K-Number: K890207 · 1989-05-31

Decision Date1989-05-31

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

INTERVENTIONAL PRODUCTS - GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is E-Z-Em, Inc.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K890207. 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 INTERVENTIONAL PRODUCTS - GUIDE WIRES?

INTERVENTIONAL PRODUCTS - GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is E-Z-Em, Inc.. The 510(k) number is K890207.

When did INTERVENTIONAL PRODUCTS - GUIDE WIRES receive FDA 510(k) clearance?

INTERVENTIONAL PRODUCTS - GUIDE WIRES received FDA 510(k) clearance on 1989-05-31, under 510(k) number K890207.

Who is the listed applicant for INTERVENTIONAL PRODUCTS - GUIDE WIRES?

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

What is the FDA product code for INTERVENTIONAL PRODUCTS - GUIDE WIRES?

The FDA product code for INTERVENTIONAL PRODUCTS - GUIDE WIRES 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.