Nidek Medical Products, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Nidek Medical Products, Inc. has 12 FDA 510(k) cleared anesthesiology devices. Based in Birmingham, US.
Historical record: 12 cleared submissions from 1988 to 2020.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nidek Medical Products, Inc.
12 devices
Cleared
May 07, 2020
Nuvo Nano Portable Oxygen Concentrator
Anesthesiology
224d
Cleared
Feb 28, 2013
MARK 5 NUVO LITE OCSI, MARK 5 NUVO LITE STD
Anesthesiology
85d
Cleared
Jan 14, 2010
MARK 5 NUVO 8 OCSI, MARK 5 NUVO 8 STD
Anesthesiology
84d
Cleared
Dec 03, 2008
MARK 5 NUVO LITE OCSI AND STD
Anesthesiology
90d
Cleared
Apr 29, 2004
MARK 5 NUVO OCSI (M5C5), MODELS 505 AND 905
Anesthesiology
23d
Cleared
Mar 18, 2004
MARK 5 NUVO (M5C5)
Anesthesiology
217d
Cleared
May 03, 2002
PULMO-MIST COMPRESSOR MODEL # 4323
Anesthesiology
52d
Cleared
Nov 17, 1998
SILENZIO DELTA CONTINUOUS POSITIVE AIRWAY PRESSURE SYSTEM
Anesthesiology
278d
Cleared
Jan 23, 1997
SILENZIO PLUS CONTINUOUS POSITIVE AIRWAY PRESSURE SYSTEM
Anesthesiology
211d
Cleared
May 07, 1996
CP-90 CONTINUOUS POSITIVE AIRWAY PRESSURE SYSTEM
Anesthesiology
315d
Cleared
May 03, 1995
OXYCHEK OXYGEN ANALYZER
Anesthesiology
336d
Cleared
Nov 02, 1988
MARK-5 CONCENTRATOR
Anesthesiology
71d