• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

  • 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 show TPLC since Back to Search Results
Device media, potentiating for in vitro diagnostic use
Regulation Description Potentiating media for in vitro diagnostic use.
Product CodeKSG
Regulation Number 864.9600
Device Class 2

MDR Year MDR Reports MDR Events
2020 1 2

Device Problems MDRs with this Device Problem Events in those MDRs
Device Markings/Labelling Problem 1 2

Patient Problems MDRs with this Patient Problem Events in those MDRs
Insufficient Information 1 2

-
-