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FDA 510(k)

MEDRAD PATHFINDER HR ROADMAPPING SYSTEM

K-Number: K914366 · 1992-02-27

ApplicantMedrad, Inc.
Decision Date1992-02-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD PATHFINDER HR ROADMAPPING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1992-02-27 under 510(k) number K914366. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD PATHFINDER HR ROADMAPPING SYSTEM?

MEDRAD PATHFINDER HR ROADMAPPING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Medrad, Inc.. The 510(k) number is K914366.

When did MEDRAD PATHFINDER HR ROADMAPPING SYSTEM receive FDA 510(k) clearance?

MEDRAD PATHFINDER HR ROADMAPPING SYSTEM received FDA 510(k) clearance on 1992-02-27, under 510(k) number K914366.

Who is the listed applicant for MEDRAD PATHFINDER HR ROADMAPPING SYSTEM?

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 MEDRAD PATHFINDER HR ROADMAPPING SYSTEM?

The FDA product code for MEDRAD PATHFINDER HR ROADMAPPING SYSTEM is LLZ.

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.

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Related Devices (Code: LLZ)

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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