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FDA 510(k)

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER

K-Number: K884375 · 1989-01-11

ApplicantArgon Medical Corp.
Decision Date1989-01-11
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSLUMBAR AORTOGRAPHY NEEDLE 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 1989-01-11 under 510(k) number K884375. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER?

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER is a medical device that received FDA 510(k) clearance on 1989-01-11. The listed applicant is Argon Medical Corp.. The 510(k) number is K884375.

When did TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER receive FDA 510(k) clearance?

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER received FDA 510(k) clearance on 1989-01-11, under 510(k) number K884375.

Who is the listed applicant for TRANSLUMBAR AORTOGRAPHY NEEDLE 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 TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER?

The FDA product code for TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER is DQR.

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Other records listing Argon Medical Corp. 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.

K904994CLOSED SYSTEM FLUSH SETK895511CATHETER BALLOON DILATOR PRESSURE GAUGEK894157OBTURATORK891022INTRODUCER FOR PTCA GUIDING CATHETERSK882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLEK871297KADIR HI-TORQUE GUIDE WIRE

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Related Devices (Code: DQR)

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.

K131446INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLESIntegra LifeSciences CorporationK07355918 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA IIEdwards Lifesciences Research MedicalK051655ANGIODYNAMICS, INC., MICRO ACCESS KITSAngioDynamics, Inc.K030398CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221Cardiacassist, Inc.K960098RMI INTERNAL MAMMARY ARTERY CANNULAResearch Medical, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.

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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