510(k) K200693

Device
K2 MOBILE
Applicant
HULASER, Inc.
510(k) number
K200693
Product code
GEX  
Decision
Substantially Equivalent (SESE)
Decision date
2020-11-19
Date received
2020-03-16
Regulation
878.4810
Classification name
Powered Laser Surgical Instrument
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
InBae Park
Address
1110, Daerung Technotown 17, 25, Gasan Digital 1-Ro, Geumcheon-Gu Seoul KR 08594 08594

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
08800079000008K2 MOBILEHULASER, Inc.2022-06-16

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Legacy Summary

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FDA Review

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