• 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 Multi-Analyte Controls, All Kinds (Assayed)
510(k) Number K992770
Device Name QUALITROL IMMUNOLOGY CONTROL, LEVEL 1, 2 AND 3
Applicant
Seracare Technology
2170 Woodward St.
Austin,  TX  78744 -1832
Applicant Contact RUSTY SEWELL
Correspondent
Seracare Technology
2170 Woodward St.
Austin,  TX  78744 -1832
Correspondent Contact RUSTY SEWELL
Regulation Number862.1660
Classification Product Code
JJY  
Date Received08/17/1999
Decision Date 11/12/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Immunology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-