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FDA 510(k)

INTERSEPT FILTERED CARDIOTOMY RESERVOIR

K-Number: K926226 · 1993-06-22

ApplicantMedtronic Vascular
Decision Date1993-06-22
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERSEPT FILTERED CARDIOTOMY RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K926226. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSEPT FILTERED CARDIOTOMY RESERVOIR?

INTERSEPT FILTERED CARDIOTOMY RESERVOIR is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Medtronic Vascular. The 510(k) number is K926226.

When did INTERSEPT FILTERED CARDIOTOMY RESERVOIR receive FDA 510(k) clearance?

INTERSEPT FILTERED CARDIOTOMY RESERVOIR received FDA 510(k) clearance on 1993-06-22, under 510(k) number K926226.

Who is the listed applicant for INTERSEPT FILTERED CARDIOTOMY RESERVOIR?

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

What is the FDA product code for INTERSEPT FILTERED CARDIOTOMY RESERVOIR?

The FDA product code for INTERSEPT FILTERED CARDIOTOMY RESERVOIR is DTZ.

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Related Devices (Code: DTZ)

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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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