Ventlab Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ventlab Corp. - FDA 510(k) Cleared Devices
Recent clearances: VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER, CUFF SENTRY, VENTLAB 6000 SERIES HUMIDIFIER
22
Total
22
Cleared
0
Denied
Ventlab Corp. has 22 FDA 510(k) cleared anesthesiology devices. Based in Hackensack, US.
Historical record: 22 cleared submissions from 1989 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ventlab Corp.
22 devices
Cleared
May 24, 2012
VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER
Anesthesiology
128d
Cleared
Jul 22, 2011
CUFF SENTRY
Anesthesiology
309d
Cleared
Jan 27, 2011
VENTLAB 6000 SERIES HUMIDIFIER
Anesthesiology
430d
Cleared
Dec 10, 2009
ACE/STATCHECK II CO2 INDICATOR, ACE/STATCHECK II CO2 INDICATOR ARM ASSEMBY...
Anesthesiology
24d
Cleared
Jun 25, 2009
VENTLAB 5000 SERIES NEBULIZER ASSEMBLY, CUP, CUP W/ MASK, CUP W/ FITSALL CONN.
Anesthesiology
90d
Cleared
Aug 13, 2008
SERIES SY DISPOSABLE ELECTROSURGICAL PAD
General & Plastic Surgery
8d
Cleared
Mar 26, 2008
VENTLAB NASAL CO2 SAMPLING/O2 DELIVERY CANNULA
Anesthesiology
460d
Cleared
Jun 03, 2004
VENTLAB NASAL CPAP CANNULA
Anesthesiology
73d
Cleared
Jul 07, 2003
VENTLAB BACTERIAL FILTER, MODEL BF100
General Hospital
161d
Cleared
Feb 11, 2002
MODIFICATION TO VENTLAB HYPERINFLATION BAG SYSTEM
Anesthesiology
14d
Cleared
Dec 20, 2001
VENTLAB HYPERINFLATION BAG SYSTEM
Anesthesiology
77d
Cleared
Sep 18, 2001
V*CARE MANUAL RESUSCITATOR
Anesthesiology
26d