• 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 instrument, quality-assurance, radiologic
Product CodeLHO
Regulation Number 892.1940
Device Class 1

MDR Year MDR Reports MDR Events
2023 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Product Quality Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Unintended Radiation Exposure 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Landauer II Mar-21-2024
2 Mevion Medical Systems, Inc. II Jul-22-2020
-
-