Creganna Medical Devices
Creganna Medical Devices holds FDA 510(k) medical device clearance, cleared in 2013, with 5 FDA device recalls on record.
Top product codes for Creganna Medical Devices
FDA recalls by Creganna Medical Devices
- Z-2249-2023 — Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access
- Z-2532-2017 — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004EPTMCA85300
- Z-2530-2017 — Boston Scientific Zurpaz(TM) MEDIUM CURL, SYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USMC85100
- Z-2531-2017 — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004EPTMCA85400
- Z-2529-2017 — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Creganna Medical Devices
Data sourced from openFDA. This site is unofficial and independent of the FDA.