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 K934808
Device Name UVISOL AND UVISOL II
Applicant
NATIONAL BIOLOGICAL CORP.
1532 ENTERPRISE PKWY.
TWINSBURG,  OH  44087
Applicant Contact FRANCIS D LAMM
Correspondent
NATIONAL BIOLOGICAL CORP.
1532 ENTERPRISE PKWY.
TWINSBURG,  OH  44087
Correspondent Contact FRANCIS D LAMM
Regulation Number878.4630
Classification Product Code
FTC  
Date Received10/07/1993
Decision Date 12/16/1993
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
-
-