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FDA 510(k)

CAPIOX CIRCUIT CONNECTORS

K-Number: K073474 · 2008-03-05

ApplicantTerumo Corp.
Decision Date2008-03-05
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAPIOX CIRCUIT CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Corp.. It received FDA 510(k) clearance on 2008-03-05 under 510(k) number K073474. 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 CAPIOX CIRCUIT CONNECTORS?

CAPIOX CIRCUIT CONNECTORS is a medical device that received FDA 510(k) clearance on 2008-03-05. The listed applicant is Terumo Corp.. The 510(k) number is K073474.

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

CAPIOX CIRCUIT CONNECTORS received FDA 510(k) clearance on 2008-03-05, under 510(k) number K073474.

Who is the listed applicant for CAPIOX CIRCUIT CONNECTORS?

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

What is the FDA product code for CAPIOX CIRCUIT CONNECTORS?

The FDA product code for CAPIOX CIRCUIT CONNECTORS is DTL.

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Other records listing Terumo Corp. 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.

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Related Devices (Code: DTL)

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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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