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

Establishment Registration & Device Listing

  • Print
  • Share
  • E-mail
-
New Search Back To Search Results
Proprietary Name: Biopsy Forceps
Classification Name: TUBING, PUMP, CARDIOPULMONARY BYPASS
Product Code: DWE
Device Class: 2
Regulation Number: 870.4390
Medical Specialty: Cardiovascular
Registered Establishment Name: CORDIS CORPORATION
Registered Establishment Number: 1016427
Owner/Operator: CORDIS CORPORATION
Owner/Operator Number: 1016427
Establishment Operations: Manufacturer; Specification Developer; Complaint File Establishment
-
-