• 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 ninhydrin and l-leucyl-l-alanine (fluorimetric), phenylalanine
510(k) Number K000754
Device Name QUANTASE PHENYLALANINE SCREENING ASSAY 500 TEST KIT
Applicant
QUANTASE LTD.
3 RIVERVIEW BUSINESS PARK
FRIARTON ROAD
PERTH, SCOTLAND,  GB PH2 8DF
Applicant Contact R. STEWART CAMPBELL
Correspondent
QUANTASE LTD.
3 RIVERVIEW BUSINESS PARK
FRIARTON ROAD
PERTH, SCOTLAND,  GB PH2 8DF
Correspondent Contact R. STEWART CAMPBELL
Regulation Number862.1555
Classification Product Code
JNB  
Date Received03/08/2000
Decision Date 06/19/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-