Inviro Medical Devices, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Inviro Medical Devices, Inc. has 7 FDA 510(k) cleared medical devices. Based in Duluth, US.
Historical record: 7 cleared submissions from 2007 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Inviro Medical Devices, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Aug 20, 2010
INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)
General Hospital
98d
Cleared
Sep 04, 2009
INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES
General Hospital
28d
Cleared
Sep 04, 2009
1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML...
General Hospital
28d
Cleared
May 15, 2009
INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022
General Hospital
142d
Cleared
Oct 22, 2008
INVIROSTRIPE 3ML, 5ML, 10ML LUER LOCK SYRINGES
General Hospital
154d
Cleared
Feb 12, 2008
INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001,...
General Hospital
279d
Cleared
Apr 23, 2007
INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022,...
General Hospital
91d