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 camera, television, endoscopic, without audio
510(k) Number K834069
Device Name ARTHROSCAN VIDEO SYSTEM
Applicant
CONCEPT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CONCEPT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4160
Classification Product Code
FWF  
Date Received11/25/1983
Decision Date 01/27/1984
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
-
-