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FDA 510(k)

EXTERNAL JUGULAR CVP CATHERIZATION KIT

K-Number: K802576 · 1980-11-12

ApplicantWillson
Decision Date1980-11-12
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EXTERNAL JUGULAR CVP CATHERIZATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Willson. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802576. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTERNAL JUGULAR CVP CATHERIZATION KIT?

EXTERNAL JUGULAR CVP CATHERIZATION KIT is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Willson. The 510(k) number is K802576.

When did EXTERNAL JUGULAR CVP CATHERIZATION KIT receive FDA 510(k) clearance?

EXTERNAL JUGULAR CVP CATHERIZATION KIT received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802576.

Who is the listed applicant for EXTERNAL JUGULAR CVP CATHERIZATION KIT?

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

What is the FDA product code for EXTERNAL JUGULAR CVP CATHERIZATION KIT?

The FDA product code for EXTERNAL JUGULAR CVP CATHERIZATION KIT is DRX.

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.

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Other records listing Willson 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.

K812143INTRODUCER, PERCUTANEOUS

Related Devices (Code: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

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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