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FDA 510(k)

CARDIOSEARCH RIGHT ATRIAL CATH-

K-Number: K833873 · 1984-06-11

ApplicantCardio Search, Inc.
Decision Date1984-06-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOSEARCH RIGHT ATRIAL CATH- is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Search, Inc.. It received FDA 510(k) clearance on 1984-06-11 under 510(k) number K833873. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOSEARCH RIGHT ATRIAL CATH-?

CARDIOSEARCH RIGHT ATRIAL CATH- is a medical device that received FDA 510(k) clearance on 1984-06-11. The listed applicant is Cardio Search, Inc.. The 510(k) number is K833873.

When did CARDIOSEARCH RIGHT ATRIAL CATH- receive FDA 510(k) clearance?

CARDIOSEARCH RIGHT ATRIAL CATH- received FDA 510(k) clearance on 1984-06-11, under 510(k) number K833873.

Who is the listed applicant for CARDIOSEARCH RIGHT ATRIAL CATH-?

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

What is the FDA product code for CARDIOSEARCH RIGHT ATRIAL CATH-?

The FDA product code for CARDIOSEARCH RIGHT ATRIAL CATH- is DQY.

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 Cardio Search, 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.

K842133EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUSK841880ERYTHROCATH UMBILICAL CATHETERK832064VENOUS CATHETER

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

Official Source

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