Hans Rudolph, Inc. is one of 18330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hans Rudolph, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HRI 6500, 6600 AND 6700 SERIES V2MASKS, 7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS, HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS
11
Total
11
Cleared
0
Denied
Hans Rudolph, Inc. has 11 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1979 to 2008.
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 - Hans Rudolph, Inc.
11 devices
Cleared
Feb 01, 2008
HRI 6500, 6600 AND 6700 SERIES V2MASKS
Anesthesiology
283d
Cleared
Jun 03, 2003
7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS
Anesthesiology
81d
Cleared
May 02, 2003
HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS
Anesthesiology
72d
Cleared
Aug 13, 2002
7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630...
Anesthesiology
159d
Cleared
Oct 16, 1996
HANS RUDOLPH NASAL CPAP MASK
Anesthesiology
86d
Cleared
Jun 20, 1996
ULTIMATE SEAL
Anesthesiology
143d
Cleared
Sep 15, 1995
DIRECTIONAL CONTROL VALVES INFLATABLE BALLOON-TYPE AND CONTROLLERS
Anesthesiology
276d
Cleared
Jan 27, 1995
MASK, GAS, ANESTHETIC
Anesthesiology
56d
Cleared
Jan 03, 1994
NONREBREATHING VALVE
Anesthesiology
164d
Cleared
Aug 20, 1993
NON CONDUCTIVE ANESTHESIA FACE MASK,SILICONE
Anesthesiology
108d
Cleared
Oct 04, 1979
4200 PNEUMATIC MOUTH SHUTTER
Anesthesiology
37d