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FDA 510(k)

Z-DOSE29

K-Number: K170273 · 2017-04-28

ApplicantZetta Medical Technologies, LLC
Decision Date2017-04-28
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Z-DOSE29 is a medical device manufactured by Zetta Medical Technologies, LLC. It received FDA 510(k) clearance on 2017-04-28 under approval number K170273. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z-DOSE29?

Z-DOSE29 is a medical device that received FDA 510(k) clearance on 2017-04-28. It is manufactured by Zetta Medical Technologies, LLC. The 510(k) number is K170273.

When was Z-DOSE29 approved by the FDA?

Z-DOSE29 received FDA 510(k) clearance on 2017-04-28, under approval number K170273.

What company makes Z-DOSE29?

Z-DOSE29 is manufactured by Zetta Medical Technologies, LLC.

What is the FDA product code for Z-DOSE29?

The FDA product code for Z-DOSE29 is JAK.

Other Devices by Zetta Medical Technologies, LLC

K160852Zia K172768ZOOM

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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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