Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name light, ultraviolet, dermatological
510(k) Number K760471
Device Name LAMP, FLOURESCENT BLACK, HIGH OUTPUT
Applicant
DERMATRON CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
DERMATRON CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4630
Classification Product Code
FTC  
Date Received08/19/1976
Decision Date 09/15/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-