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FDA 510(k)

BENZALKONIUM-HEPARIN COATED GUIDEWIRES

K-Number: K802473 · 1980-11-12

ApplicantMedrad, Inc.
Decision Date1980-11-12
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BENZALKONIUM-HEPARIN COATED GUIDEWIRES is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802473. 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 BENZALKONIUM-HEPARIN COATED GUIDEWIRES?

BENZALKONIUM-HEPARIN COATED GUIDEWIRES is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Medrad, Inc.. The 510(k) number is K802473.

When did BENZALKONIUM-HEPARIN COATED GUIDEWIRES receive FDA 510(k) clearance?

BENZALKONIUM-HEPARIN COATED GUIDEWIRES received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802473.

Who is the listed applicant for BENZALKONIUM-HEPARIN COATED GUIDEWIRES?

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

What is the FDA product code for BENZALKONIUM-HEPARIN COATED GUIDEWIRES?

The FDA product code for BENZALKONIUM-HEPARIN COATED GUIDEWIRES is DQX.

Related Clinical Trials

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.

Other records listing Medrad, Inc. as applicant

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.

View all 104 devices →

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.

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.

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