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 Bromcresol Green Dye-Binding, Albumin
510(k) Number K943000
Device Name ALBUMIN QVET
Applicant
PRISMA SYSTEMS
1721 BLACK RIVER BLVD.
SUITE 200
ROME,  NY  13440
Applicant Contact LARRY J BEASLEY
Correspondent
PRISMA SYSTEMS
1721 BLACK RIVER BLVD.
SUITE 200
ROME,  NY  13440
Correspondent Contact LARRY J BEASLEY
Regulation Number862.1035
Classification Product Code
CIX  
Date Received06/23/1994
Decision Date 12/13/1994
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
-
-