Aesculap, Inc. - FDA 510(k) Cleared Devices
207
Total
201
Cleared
0
Denied
FDA 510(k) cleared devices by Aesculap, Inc. General Hospital ✕
17 devices
Cleared
May 13, 2025
Aesculap Aicon® Series Container System
General Hospital
243d
Cleared
Dec 30, 2022
Aesculap AICON Container
General Hospital
372d
Cleared
Mar 27, 2020
JJ Series Container System
General Hospital
239d
Cleared
Mar 17, 2020
SterilContainer S2 System
General Hospital
85d
Cleared
Jul 05, 2019
Aesculap® SterilContainer(TM) S2 System
General Hospital
304d
Cleared
Dec 21, 2018
SterilContainer S System
General Hospital
144d
Cleared
Nov 17, 2017
SterilContainer with PrimeLine Pro Lid
General Hospital
58d
Cleared
Jul 13, 2017
SterilContainer S System
General Hospital
280d
Cleared
Oct 09, 2015
SterilContainer S
General Hospital
151d
Cleared
Aug 18, 2015
SterilContainer S
General Hospital
232d
Cleared
Jul 08, 2015
SterilContainer S System
General Hospital
267d
Cleared
Jul 27, 2010
AESCULAP STERILCONTAINER S
General Hospital
259d
Cleared
Apr 28, 2008
AESCULAP PRIMELINE CONTAINER LTD.
General Hospital
171d
Cleared
Jul 31, 2006
CELSITE/ CELSITE CONCEPT, ACCESS PORTS
General Hospital
69d
Cleared
Feb 15, 2006
AESCULAP STERILCONTAINER SYSTEM
General Hospital
72d
Cleared
Dec 13, 2004
REUSABLE STERILCONTAINER FILTER MODEL #JK090
General Hospital
180d
Cleared
Feb 09, 1994
MIS CLEAN-SET FLUSHING UNIT AND ACCESSORIES
General Hospital
217d