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FDA 510(k)

STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES

K-Number: K914531 · 1992-02-27

ApplicantArrow Intl., Inc.
Decision Date1992-02-27
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1992-02-27 under 510(k) number K914531. 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 STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES?

STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K914531.

When did STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES receive FDA 510(k) clearance?

STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES received FDA 510(k) clearance on 1992-02-27, under 510(k) number K914531.

Who is the listed applicant for STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES?

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

What is the FDA product code for STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES?

The FDA product code for STAINLESS STEEL GEN PUR INTERVENTIONAL GUIDE WIRES is DQX.

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Related Devices (Code: DQX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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