FDA Product Code LWE: Bone Marrow Collection/transfusion Kit
This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Www.fda.gov/cdrh/ode/convkit.html.this Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.
Leading manufacturers include Baxter Healthcare Corp, Proact, Ltd. and Promedical , Ltd..
3
Total
3
Cleared
128d
Avg days
1987
Since
FDA 510(k) Cleared Bone Marrow Collection/transfusion Kit Devices (Product Code LWE)
3 devices
Cleared
Jul 17, 1995
JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)
Promedical , Ltd.
General Hospital
59d
Cleared
Nov 01, 1991
BONE-TEMNO/STERNUM-TEMNO
Proact, Ltd.
General Hospital
99d
Cleared
Nov 06, 1987
BONE MARROW COLLECTION KIT AND STAND
Baxter Healthcare Corp
General Hospital
227d