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FDA 510(k)

ZIIP+ Device

K-Number: K212342 · 2021-09-23

ApplicantZiip, Inc.
Decision Date2021-09-23
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZIIP+ Device is a medical device manufactured by Ziip, Inc.. It received FDA 510(k) clearance on 2021-09-23 under approval number K212342. 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 2021-09-23. It is manufactured by Ziip, Inc.. The 510(k) number is K212342.

When was ZIIP+ Device approved by the FDA?

ZIIP+ Device received FDA 510(k) clearance on 2021-09-23, under approval number K212342.

What company makes ZIIP+ Device?

ZIIP+ Device is manufactured by Ziip, Inc..

What is the FDA product code for ZIIP+ Device?

The FDA product code for ZIIP+ Device is NFO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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