Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K132838
Device Classification Name
Over-The-Counter Powered Light Based Laser For Acne
More FDA Info for this Device
510(K) Number
K132838
Device Name
Over-The-Counter Powered Light Based Laser For Acne
Applicant
NUTRA LUXE MD, LLC
5575 SANTA ROSA CT.
SPARKS, NV 89436 US
Other 510(k) Applications for this Company
Contact
JILL CREASY
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
OLP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/10/2013
Decision Date
05/23/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact