Clearmedical, Inc. is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clearmedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS, REPROCESSED MULTIPLE CLIP APPLIERS, REPROCESSED TROCARS
14
Total
14
Cleared
0
Denied
Clearmedical, Inc. has 14 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Historical record: 14 cleared submissions from 2002 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Clearmedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Clearmedical, Inc.
14 devices
Cleared
Jul 11, 2005
REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS
General & Plastic Surgery
606d
Cleared
Jul 11, 2005
REPROCESSED MULTIPLE CLIP APPLIERS
General & Plastic Surgery
606d
Cleared
Jun 03, 2005
REPROCESSED TROCARS
Ear, Nose, Throat
568d
Cleared
Jul 27, 2004
REPROCESSED SURGICAL SCISSORS AND GRASPERS
General & Plastic Surgery
257d
Cleared
Nov 20, 2003
REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS
Gastroenterology & Urology
7d
Cleared
Jul 15, 2003
CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF
Cardiovascular
71d
Cleared
Jul 03, 2002
CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25L
Anesthesiology
324d
Cleared
Jul 03, 2002
CLEARMEDICAL/NELLCOR OXISENSOR II, NEONATAL/ADULT, MODEL N-25
Anesthesiology
324d
Cleared
Jul 03, 2002
CLEARMEDICAL/NELLCOR OXISENSOR II, PEDIATRIC, MODEL D-20
Anesthesiology
324d
Cleared
Feb 06, 2002
CLEARMEDICAL/AIRCAST VENAFLOW CALF CUFF, CLEARMEDICAL AIRCAST XL VENAFLOW...
Cardiovascular
177d
Cleared
Feb 06, 2002
CLEARMEDICAL/KENDALL KNEE-HIGH SCD SLEEVES, CLEARMEDICAL/KENDALL THIGH-HIGH...
Cardiovascular
177d
Cleared
Feb 06, 2002
CLEARMEDICAL/NOVAMEDIX AVI FOOT COVER, PAIR, REGULAR & LARGE SIZE
Cardiovascular
177d