• 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 Bromcresol Green Dye-Binding, Albumin
510(k) Number K850931
Device Name ALBUMIN
Applicant
Dilab, Inc.
7003 NW 50th St.
Miami,  FL  33166
Applicant Contact RAFAEL A QUEVEDO
Correspondent
Dilab, Inc.
7003 NW 50th St.
Miami,  FL  33166
Correspondent Contact RAFAEL A QUEVEDO
Regulation Number862.1035
Classification Product Code
CIX  
Date Received03/07/1985
Decision Date 06/26/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-