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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 the device name listed in this FDA 510(k) record. The listed applicant is Conversion Labs, Pr, LLC. It received FDA 510(k) clearance on 2020-03-25 under 510(k) 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. The listed applicant is Conversion Labs, Pr, LLC. The 510(k) number is K193667.

When did Shapiro MD model laser 272 receive FDA 510(k) clearance?

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

Who is the listed applicant for Shapiro MD model laser 272?

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

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

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

Related Devices (Code: OAP)

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.

Official Source

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