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 Control, Hematocrit
510(k) Number K893562
Device Name A.QC HCT LEVEL 1 AND 2
Applicant
Johnson & Johnson Professionals, Inc.
2675 Long Lake Rd.
Roseville,  MN  55113
Applicant Contact PETER J CORDON
Correspondent
Johnson & Johnson Professionals, Inc.
2675 Long Lake Rd.
Roseville,  MN  55113
Correspondent Contact PETER J CORDON
Regulation Number864.8625
Classification Product Code
GLK  
Date Received05/09/1989
Decision Date 07/14/1989
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
-
-