Rondex Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rondex Products, Inc. - FDA 510(k) Cleared Devices
11
Total
10
Cleared
0
Denied
Rondex Products, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1984 to 1998.
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) Regulatory Record - Rondex Products, Inc.
11 devices
Cleared
May 19, 1998
RONDEX CPR ISO-SHIELD
Anesthesiology
50d
Cleared
Feb 07, 1995
CPR SHIELD
Anesthesiology
246d
Cleared
Nov 10, 1994
NON-BREATHING VALVE
Anesthesiology
100d
Cleared
Oct 06, 1992
RONDEX MASK MODELS 9122/9111/9102/911102, MODIFIED
Anesthesiology
224d
Cleared
Nov 08, 1991
RONDEX CPR NON REBREATHING VALVE #9030, MODIFIED
Anesthesiology
64d
Cleared
Nov 08, 1991
RONDEX MASKS MODELS 9015/9011/901102 MODIFIED
Anesthesiology
64d
Cleared
Oct 26, 1990
CPR VALVE (NON-REBREATHING) MODEL #9030
Anesthesiology
157d
Cleared
Aug 22, 1990
ORAL-NASAL MASK RESUSCITATION AND ANESTHETIC GAS
Anesthesiology
92d
Cleared
Jul 21, 1988
RESCUE MASK & CPR VALVE FOR MOUTH-TO-MASK TYPE CPR
Anesthesiology
73d
Cleared
Apr 25, 1988
RONDEX RESCUE MASK
Anesthesiology
21d
Cleared
Jan 18, 1984
RESCUE MASK
Anesthesiology
42d