• 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 Chromatographic, Phospholipids
510(k) Number K914040
Device Name PHOSPHOLIPID REAGENT SET
Applicant
Sterling Diagnostics, Inc.
6226 Product Dr.
Sterling Heights,  MI  48312
Applicant Contact DAVID L CALLENDER
Correspondent
Sterling Diagnostics, Inc.
6226 Product Dr.
Sterling Heights,  MI  48312
Correspondent Contact DAVID L CALLENDER
Regulation Number862.1575
Classification Product Code
JNT  
Date Received09/10/1991
Decision Date 10/30/1991
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
-
-