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FDA 510(k)

Dermapose Refresh

K-Number: K193363 · 2020-04-14

ApplicantPuregraft, LLC
Decision Date2020-04-14
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Dermapose Refresh is the device name listed in this FDA 510(k) record. The listed applicant is Puregraft, LLC. It received FDA 510(k) clearance on 2020-04-14 under 510(k) 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. The listed applicant is Puregraft, LLC. The 510(k) number is K193363.

When did Dermapose Refresh receive FDA 510(k) clearance?

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

Who is the listed applicant for Dermapose Refresh?

The FDA 510(k) record lists Puregraft, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dermapose Refresh?

The FDA product code for Dermapose Refresh is MUU.

Other records listing Puregraft, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K200168Dermapose Access

Related Devices (Code: MUU)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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