FDA 510(k)

Dermapose Refresh

K-Number: K193363 · 2020-04-14

Decision Date2020-04-14

Product CodeMUU

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Dermapose Refresh is a medical device manufactured by Puregraft, LLC. It received FDA 510(k) clearance on 2020-04-14 under approval number K193363. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dermapose Refresh?

Dermapose Refresh is a medical device that received FDA 510(k) clearance on 2020-04-14. It is manufactured by Puregraft, LLC. The 510(k) number is K193363.

When was Dermapose Refresh approved by the FDA?

Dermapose Refresh received FDA 510(k) clearance on 2020-04-14, under approval number K193363.

What company makes Dermapose Refresh?

Dermapose Refresh is manufactured by Puregraft, LLC.

What is the FDA product code for Dermapose Refresh?

The FDA product code for Dermapose Refresh is MUU.

Other Devices by Puregraft, LLC

K200168Dermapose Access

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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.