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FDA 510(k)

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup

K-Number: K181253 · 2018-08-10

ApplicantPjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC
Decision Date2018-08-10
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is a medical device manufactured by Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC. It received FDA 510(k) clearance on 2018-08-10 under approval number K181253. 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 Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is a medical device that received FDA 510(k) clearance on 2018-08-10. It is manufactured by Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC. The 510(k) number is K181253.

When was Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup approved by the FDA?

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup received FDA 510(k) clearance on 2018-08-10, under approval number K181253.

What company makes Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is manufactured by Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC.

What is the FDA product code for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

The FDA product code for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is OAP.

Other Devices by Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC

K192585Bosley Revitalizer 96 Laser Cap, Bosley Revitalizer 96 XL Laser Cap

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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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