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FDA 510(k)

TERUMO LAUER LOCK ADAPTER

K-Number: K093992 · 2010-05-19

ApplicantTerumo Cardiovascular Systems Corporation
Decision Date2010-05-19
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TERUMO LAUER LOCK ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Cardiovascular Systems Corporation. It received FDA 510(k) clearance on 2010-05-19 under 510(k) number K093992. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERUMO LAUER LOCK ADAPTER?

TERUMO LAUER LOCK ADAPTER is a medical device that received FDA 510(k) clearance on 2010-05-19. The listed applicant is Terumo Cardiovascular Systems Corporation. The 510(k) number is K093992.

When did TERUMO LAUER LOCK ADAPTER receive FDA 510(k) clearance?

TERUMO LAUER LOCK ADAPTER received FDA 510(k) clearance on 2010-05-19, under 510(k) number K093992.

Who is the listed applicant for TERUMO LAUER LOCK ADAPTER?

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

What is the FDA product code for TERUMO LAUER LOCK ADAPTER?

The FDA product code for TERUMO LAUER LOCK ADAPTER is DTL.

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Other records listing Terumo Cardiovascular Systems Corporation as applicant

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K234065CDI OneView Monitoring SystemK221895Terumo Advanced Perfusion System 1K200091Capiox iCP Centrifugal PumpK182110CDI Blood Parameter Monitoring System 550K180950Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo Capiox NX19 Oxygenator with Reservoir (west Orientation), Terumo Capiox NX19 Oxygenator (east Orientation), Terumo Capiox NX19 Oxygenator (west Orientation)K172071Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo Capiox NX19 Oxygenator with Reservoir (west orientation ), Terumo Capiox NX19 Oxygenator (east orientation ), Terumo Capiox NX19 Oxygenator (west orientation)

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Related Devices (Code: DTL)

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.

K131124COLIGNJilin Coronado Medical , Ltd.K123448AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH BALANCE BIOSURFACE, AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH CARMEDA BIOACTIVEMedtronic, Inc.K122811CONNECTOR COMPONENTS WITH BALANCE BIOSURFACEMedtronic, Inc.K122301GUARDIAN II HEMOSTASIS VALVE GUARDIAN II NC HEMOSTASIS VALVEVascular Solutions Zerusa , Ltd.K120069MEDLINE STOPCOCK AND MANIFOLDMedline Industries, Inc.K113148E-PASSSynexmed(Shenzhen)Company Limited

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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