Getinge/Castle, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Getinge/Castle, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Getinge/Castle, Inc. has 9 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 9 cleared submissions from 1997 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Getinge/Castle, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Getinge/Castle, Inc.
9 devices
Cleared
Jun 24, 2002
CASTLE PERACETIC ACID BIOLOGICAL INDICATOR KIT
General Hospital
153d
Cleared
Mar 20, 2002
MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER
General Hospital
26d
Cleared
Sep 05, 2001
CASTLE 400HC/500HC SERIES STEAM STERILIZER, MODELS 422HC, 433HC, 522HC, AND...
General Hospital
27d
Cleared
Jan 02, 2001
CASTLE MODEL 233HC STEAM STERILIZER
General Hospital
57d
Cleared
Feb 16, 2000
CASTLE SERIES 100HC STEAM STERILIZERS
General Hospital
56d
Cleared
Nov 08, 1999
CASTLE SURGICAL LIGHT, MODEL 3000
General & Plastic Surgery
42d
Cleared
Mar 03, 1998
GETINGE/CASTLE OPTIVIEW SERIES SURGICAL LIGHT
General & Plastic Surgery
125d
Cleared
Feb 10, 1998
CASTLE SERIES 200 STEAM STERILIZER (POWERCLAVE)
General Hospital
167d
Cleared
Nov 12, 1997
CASTLE SERIES 100 STEAM STERILIZERS (STRAIGHTLINE)
General Hospital
246d