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 clamp, uterine
Product CodeHGC
Regulation Number 884.4520
Device Class 1

MDR Year MDR Reports MDR Events
2016 1 1
2017 4 4
2019 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Detachment Of Device Component 4 4
Device-Device Incompatibility 2 2
Break 1 1
Fracture 1 1
Stretched 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Consequences Or Impact To Patient 4 4
No Known Impact Or Consequence To Patient 2 2

Recalls
Manufacturer Recall Class Date Posted
1 Boston Scientific Corporation, Neurovascular, 47900 Bayside Parkway, Fremont, CA 94538 II Jan-05-2011
-
-