Medical Device Manufacturer · US , Mchenry , IL

Hans Rudolph, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1979

Total

Cleared

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

1-11 of 11

Cleared Feb 01, 2008

HRI 6500, 6600 AND 6700 SERIES V2MASKS

K071149 · BZD

Anesthesiology · 283d

Cleared Jun 03, 2003

7600 SERIES MULTI-PATIENT MULTI-USE ORO-NASAL CPAP/NPPV MASKS

K030822 · BZD

Anesthesiology · 81d

Cleared May 02, 2003

HANS RUDOLPH 7500 SERIES REUSABLE ORO-NASAL NIV MASKS

K030515 · CBK

Anesthesiology · 72d

Cleared Aug 13, 2002

7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630...

K020759 · BZD

Anesthesiology · 159d

Cleared Oct 16, 1996

HANS RUDOLPH NASAL CPAP MASK

Anesthesiology · 143d

Cleared Sep 15, 1995

DIRECTIONAL CONTROL VALVES INFLATABLE BALLOON-TYPE AND CONTROLLERS

K946077 · BZC

Anesthesiology · 276d

Cleared Jan 27, 1995

MASK, GAS, ANESTHETIC

Anesthesiology · 164d

Cleared Aug 20, 1993

NON CONDUCTIVE ANESTHESIA FACE MASK,SILICONE

K932147 · BSJ

Anesthesiology · 108d

Cleared Oct 04, 1979

4200 PNEUMATIC MOUTH SHUTTER

K791705 · CCM

Anesthesiology · 37d

Hans Rudolph, Inc. - FDA 510(k) Cleared Devices

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