QUADROX-i Adult/Small Adult Oxygenators;QUADROX-iD Adult Oxygenators

FDA 510(k) K150267 · Maquet Cardiopulmonary, AG

Substantially Equivalent

510(k) numberK150267

Submission

Device name
QUADROX-i Adult/Small Adult Oxygenators;QUADROX-iD Adult Oxygenators
Applicant
Maquet Cardiopulmonary, AG
Rastatt De-Bw, DE
Received
February 4, 2015
Decision date
May 7, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTZ – Oxygenator, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4350
Specialty
Cardiovascular
Life-sustaining
Yes

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Questions and answers

When was QUADROX-i Adult/Small Adult Oxygenators;QUADROX-iD Adult Oxygenators cleared by the FDA?

QUADROX-i Adult/Small Adult Oxygenators;QUADROX-iD Adult Oxygenators (K150267) received a 510(k) decision of Substantially Equivalent on May 7, 2015, 92 days after the submission was received.

What is the product code of K150267?

The FDA product code is DTZ – Oxygenator, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4350.