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FDA 510(k)

ZIIP Device

K-Number: K161484 · 2017-02-24

ApplicantZiip,Llc
Decision Date2017-02-24
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZIIP Device is a medical device manufactured by Ziip,Llc. It received FDA 510(k) clearance on 2017-02-24 under approval number K161484. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIIP Device?

ZIIP Device is a medical device that received FDA 510(k) clearance on 2017-02-24. It is manufactured by Ziip,Llc. The 510(k) number is K161484.

When was ZIIP Device approved by the FDA?

ZIIP Device received FDA 510(k) clearance on 2017-02-24, under approval number K161484.

What company makes ZIIP Device?

ZIIP Device is manufactured by Ziip,Llc.

What is the FDA product code for ZIIP Device?

The FDA product code for ZIIP Device is NFO.

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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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