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 Test, Qualitative And Quantitative Factor Deficiency
510(k) Number K023990
Device Name CHROMOCHECK PROTEIN C 25; CHROMOCHECK PROTEIN C 50
Applicant
Precision Biologic
900 Windmill Rd., Suite 100
Dartmouth, N.S.,  CA B3B 1P7
Applicant Contact STEPHEN L DUFF
Correspondent
Precision Biologic
900 Windmill Rd., Suite 100
Dartmouth, N.S.,  CA B3B 1P7
Correspondent Contact STEPHEN L DUFF
Regulation Number864.7290
Classification Product Code
GGP  
Date Received12/03/2002
Decision Date 03/19/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-