FDA 510(k) Applications Submitted by KEVIN RUDOLPH
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960401 |
01/29/1996 |
ULTIMATE SEAL |
HANS RUDOLPH, INC. |
| K030515 |
02/19/2003 |
HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS |
HANS RUDOLPH, INC. |
| K020759 |
03/07/2002 |
7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630 MEDIUM, 7640 SMALL, 7650 EXTRA SMALL, 7660 PETIT |
HANS RUDOLPH, INC. |
| K030822 |
03/14/2003 |
7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS |
HANS RUDOLPH, INC. |
| K071149 |
04/24/2007 |
HRI 6500, 6600 AND 6700 SERIES V2MASKS |
HANS RUDOLPH, INC. |
| K962848 |
07/22/1996 |
HANS RUDOLPH NASAL CPAP MASK |
HANS RUDOLPH, INC. |
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