Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 test, epithelial ovarian tumor associated antigen (he4)
Regulation Description Tumor-associated antigen immunological test system.
Definition An enzyme immunometric assay for the quantitative determination of HE4 in human serum. The assay is to be used as an aid in monitoring recurrence or progressive disease in patients with epithelial ovarian cancer. Serial testing for patient HE4 assay values should be used in conjunction with other clinical methods used for monitoring ovarian cancer. It is not intended to estimate or assess the risk of disease outcomes of patients.
Product CodeOIU
Regulation Number 866.6010
Device Class 2

MDR Year MDR Reports MDR Events
2022 2 2
2023 1 1
2024 1 1
2025 1 1
2026 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
High Test Results 3 3
Low Test Results 3 3
Incorrect Measurement 2 2
Non Reproducible Results 1 1
Audible Prompt/Feedback Problem 1 1
Low Readings 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 7 7

-
-