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FDA 510(k)

TERUMO ASPRIATION CATHETER

K-Number: K112382 · 2011-12-14

ApplicantTerumo Medical Corporation
Decision Date2011-12-14
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TERUMO ASPRIATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corporation. It received FDA 510(k) clearance on 2011-12-14 under 510(k) number K112382. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERUMO ASPRIATION CATHETER?

TERUMO ASPRIATION CATHETER is a medical device that received FDA 510(k) clearance on 2011-12-14. The listed applicant is Terumo Medical Corporation. The 510(k) number is K112382.

When did TERUMO ASPRIATION CATHETER receive FDA 510(k) clearance?

TERUMO ASPRIATION CATHETER received FDA 510(k) clearance on 2011-12-14, under 510(k) number K112382.

Who is the listed applicant for TERUMO ASPRIATION CATHETER?

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

What is the FDA product code for TERUMO ASPRIATION CATHETER?

The FDA product code for TERUMO ASPRIATION CATHETER is QEZ.

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Related Devices (Code: QEZ)

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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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