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Hans Rudolph, Inc.

11 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
HRI 6500, 6600 AND 6700 SERIES V2MASKS (K071149)Hans Rudolph, Inc.2008-02-01
7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS (K030822)Hans Rudolph, Inc.2003-06-03
HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS (K030515)Hans Rudolph, Inc.2003-05-02
7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630 MEDIUM, 7640 SMALL, 7650 EXTRA SMALL, 7660 PETIT (K020759)Hans Rudolph, Inc.2002-08-13
HANS RUDOLPH NASAL CPAP MASK (K962848)Hans Rudolph, Inc.1996-10-16
ULTIMATE SEAL (K960401)Hans Rudolph, Inc.1996-06-20
DIRECTIONAL CONTROL VALVES INFLATABLE BALLOON-TYPE AND CONTROLLERS (K946077)Hans Rudolph, Inc.1995-09-15
MASK, GAS, ANESTHETIC (K945894)Hans Rudolph, Inc.1995-01-27
NONREBREATHING VALVE (K933583)Hans Rudolph, Inc.1994-01-03
NON CONDUCTIVE ANESTHESIA FACE MASK,SILICONE (K932147)Hans Rudolph, Inc.1993-08-20
4200 PNEUMATIC MOUTH SHUTTER (K791705)Hans Rudolph, Inc.1979-10-04

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Every clearance here is in the API, with alerts when new ones post.