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FDA 510(k)

PATHFINDER CARDIOVASCULAR CATHETER

K-Number: K844555 · 1985-03-27

ApplicantArgon Medical Corp.
Decision Date1985-03-27
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATHFINDER CARDIOVASCULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1985-03-27 under 510(k) number K844555. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATHFINDER CARDIOVASCULAR CATHETER?

PATHFINDER CARDIOVASCULAR CATHETER is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Argon Medical Corp.. The 510(k) number is K844555.

When did PATHFINDER CARDIOVASCULAR CATHETER receive FDA 510(k) clearance?

PATHFINDER CARDIOVASCULAR CATHETER received FDA 510(k) clearance on 1985-03-27, under 510(k) number K844555.

Who is the listed applicant for PATHFINDER CARDIOVASCULAR CATHETER?

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

What is the FDA product code for PATHFINDER CARDIOVASCULAR CATHETER?

The FDA product code for PATHFINDER CARDIOVASCULAR CATHETER is DQO.

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Other records listing Argon Medical Corp. as applicant

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K904994CLOSED SYSTEM FLUSH SETK895511CATHETER BALLOON DILATOR PRESSURE GAUGEK894157OBTURATORK891022INTRODUCER FOR PTCA GUIDING CATHETERSK884375TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETERK882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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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