Hans Rudolph, Inc.
Hans Rudolph, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2008.
Top product codes for Hans Rudolph, Inc.
Recent clearances by Hans Rudolph, Inc.
- K071149 — HRI 6500, 6600 AND 6700 SERIES V2MASKS
- K030822 — 7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS
- K030515 — HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS
- K020759 — 7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630 MEDIUM, 7640 SMALL, 7650 EXTRA SMALL, 7660 PETIT
- K962848 — HANS RUDOLPH NASAL CPAP MASK
- K960401 — ULTIMATE SEAL
- K946077 — DIRECTIONAL CONTROL VALVES INFLATABLE BALLOON-TYPE AND CONTROLLERS
- K945894 — MASK, GAS, ANESTHETIC
- K933583 — NONREBREATHING VALVE
- K932147 — NON CONDUCTIVE ANESTHESIA FACE MASK,SILICONE
- K791705 — 4200 PNEUMATIC MOUTH SHUTTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.