Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup
K-Number: K181253 · 2018-08-10
Device Summary
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. The listed applicant is Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC. The 510(k) number is K181253.
When did Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup receive FDA 510(k) clearance?
Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup received FDA 510(k) clearance on 2018-08-10, under 510(k) number K181253.
Who is the listed applicant for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?
The FDA 510(k) record lists Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC as the applicant. This does not by itself establish the device manufacturer.
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 records listing Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.