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FDA 510(k)

CRITIKON TRIPLE-LUMEN CENTRAL VENOUS

K-Number: K842316 · 1984-07-20

ApplicantCritikon Company, LLC
Decision Date1984-07-20
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CRITIKON TRIPLE-LUMEN CENTRAL VENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Critikon Company, LLC. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842316. 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 CRITIKON TRIPLE-LUMEN CENTRAL VENOUS?

CRITIKON TRIPLE-LUMEN CENTRAL VENOUS is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is Critikon Company, LLC. The 510(k) number is K842316.

When did CRITIKON TRIPLE-LUMEN CENTRAL VENOUS receive FDA 510(k) clearance?

CRITIKON TRIPLE-LUMEN CENTRAL VENOUS received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842316.

Who is the listed applicant for CRITIKON TRIPLE-LUMEN CENTRAL VENOUS?

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

What is the FDA product code for CRITIKON TRIPLE-LUMEN CENTRAL VENOUS?

The FDA product code for CRITIKON TRIPLE-LUMEN CENTRAL VENOUS is DQY.

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Other records listing Critikon Company, LLC as applicant

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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.

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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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