Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by LASERLITE, LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980142
01/15/1998
FEATHERLITE DIODE LASER
LASERLITE, LLC.
K981090
03/26/1998
LASERLITE DIODE SURGICAL LASER
LASERLITE, LLC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact