Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Amaya De Levie
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180597
03/06/2018
AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO
Lumenis Ltd.
K170179
01/19/2017
LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity
Lumenis Ltd.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact