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FDA 510(k)

MaxZero Extension Sets with Needless Connector

K-Number: K171957 · 2017-07-19

ApplicantCarefusion 303, Inc.
Decision Date2017-07-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MaxZero Extension Sets with Needless Connector is a medical device manufactured by Carefusion 303, Inc.. It received FDA 510(k) clearance on 2017-07-19 under approval number K171957. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MaxZero Extension Sets with Needless Connector?

MaxZero Extension Sets with Needless Connector is a medical device that received FDA 510(k) clearance on 2017-07-19. It is manufactured by Carefusion 303, Inc.. The 510(k) number is K171957.

When was MaxZero Extension Sets with Needless Connector approved by the FDA?

MaxZero Extension Sets with Needless Connector received FDA 510(k) clearance on 2017-07-19, under approval number K171957.

What company makes MaxZero Extension Sets with Needless Connector?

MaxZero Extension Sets with Needless Connector is manufactured by Carefusion 303, Inc..

What is the FDA product code for MaxZero Extension Sets with Needless Connector?

The FDA product code for MaxZero Extension Sets with Needless Connector is FPA.

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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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