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 Counter, Urine Particle
510(k) Number K822823
Device Name HEMATOLOGY COMPUTER-INTERFACE, VISCOUNT
Applicant
Eko Scann AB
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Eko Scann AB
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.5200
Classification Product Code
LKM  
Date Received09/21/1982
Decision Date 10/18/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-