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FDA 510(k)

TERUMO CIRCUIT CONNECTORS

K-Number: K041697 · 2004-08-11

ApplicantTerumo Cardiovascular Systems Corporation
Decision Date2004-08-11
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TERUMO CIRCUIT CONNECTORS 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 2004-08-11 under 510(k) number K041697. 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 CIRCUIT CONNECTORS?

TERUMO CIRCUIT CONNECTORS is a medical device that received FDA 510(k) clearance on 2004-08-11. The listed applicant is Terumo Cardiovascular Systems Corporation. The 510(k) number is K041697.

When did TERUMO CIRCUIT CONNECTORS receive FDA 510(k) clearance?

TERUMO CIRCUIT CONNECTORS received FDA 510(k) clearance on 2004-08-11, under 510(k) number K041697.

Who is the listed applicant for TERUMO CIRCUIT CONNECTORS?

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 CIRCUIT CONNECTORS?

The FDA product code for TERUMO CIRCUIT CONNECTORS is DTL.

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Other records listing Terumo Cardiovascular Systems Corporation as applicant

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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.

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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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