• 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 slides, microscope
Regulation Description Tissue processing equipment.
Product CodeKEW
Regulation Number 864.3010
Device Class 1

MDR Year MDR Reports MDR Events
2021 1 1
2022 1 1
2024 2 2
2025 10 10

Device Problems MDRs with this Device Problem Events in those MDRs
Insufficient Information 10 10
Adverse Event Without Identified Device or Use Problem 4 4
Incorrect, Inadequate or Imprecise Result or Readings 1 1
Appropriate Term/Code Not Available 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 8 8
Insufficient Information 5 5
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 1 1

-
-