FDA 510(k)

Shapiro MD model laser 272

K-Number: K193667 · 2020-03-25

Decision Date2020-03-25

Product CodeOAP

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Shapiro MD model laser 272 is a medical device manufactured by Conversion Labs, Pr, LLC. It received FDA 510(k) clearance on 2020-03-25 under approval number K193667. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Shapiro MD model laser 272?

Shapiro MD model laser 272 is a medical device that received FDA 510(k) clearance on 2020-03-25. It is manufactured by Conversion Labs, Pr, LLC. The 510(k) number is K193667.

When was Shapiro MD model laser 272 approved by the FDA?

Shapiro MD model laser 272 received FDA 510(k) clearance on 2020-03-25, under approval number K193667.

What company makes Shapiro MD model laser 272?

Shapiro MD model laser 272 is manufactured by Conversion Labs, Pr, LLC.

What is the FDA product code for Shapiro MD model laser 272?

The FDA product code for Shapiro MD model laser 272 is OAP.

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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.