The following data is part of a premarket notification filed by Erchonia Medical, Inc. with the FDA for Erchonia Eml Laser.
Device ID | K072206 |
510k Number | K072206 |
Device Name: | ERCHONIA EML LASER |
Classification | Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy |
Applicant | ERCHONIA MEDICAL, INC. 13 RED FOX LANE Littleton, CO 80127 |
Contact | Kevin Walls |
Correspondent | Kevin Walls ERCHONIA MEDICAL, INC. 13 RED FOX LANE Littleton, CO 80127 |
Product Code | NHN |
CFR Regulation Number | 890.5500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-08-08 |
Decision Date | 2008-04-24 |