Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by PHOTOMEDEX, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082721
09/17/2008
LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS
PHOTOMEDEX, INC.
K040234
02/02/2004
LASERPRO CO2 CARBON DIOXIDE LASER SYSTEM
PHOTOMEDEX, INC.
K040294
02/06/2004
LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980
PHOTOMEDEX, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact