8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
NAMIC ONE PART INTRODUCER NEEDLE
FDA 510(k)
FDA Class 2
·Cardiovascular
SCM CATH ( SIZES ARE VARYING BETWEEN 16G X 2'' AND 24G X 3/4'' ), MODEL 1.50, 1.77,1.88',2, 1.25, 1.50, 1.77,
FDA 510(k)
FDA Class 2
·General Hospital
IMMUNOSTAT T3 UPTAKE TEST
FDA 510(k)SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 13, 2014
SPARC SLING SYSTEM
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·December 5, 2012
AORTIC AP
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWQ·June 26, 2015
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020