Medical Device Manufacturer · US , Mchenry , IL

Rondex Products, Inc. - FDA 510(k) Cleared Devices

11 submissions · 10 cleared · Since 1984

Total

Cleared

Denied

Rondex Products, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1984 to 1998.

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 - Rondex Products, Inc.

11 devices

1-11 of 11

Cleared May 19, 1998

RONDEX CPR ISO-SHIELD

Anesthesiology · 246d

Cleared Nov 10, 1994

NON-BREATHING VALVE

K943761 · CBP

Anesthesiology · 100d

Cleared Oct 06, 1992

RONDEX MASK MODELS 9122/9111/9102/911102, MODIFIED

K921002 · BTM

Anesthesiology · 224d

Cleared Nov 08, 1991

RONDEX CPR NON REBREATHING VALVE #9030, MODIFIED

K914195 · CBP

Anesthesiology · 64d

Cleared Nov 08, 1991

RONDEX MASKS MODELS 9015/9011/901102 MODIFIED

K914196 · BTM

Anesthesiology · 64d

Cleared Oct 26, 1990

CPR VALVE (NON-REBREATHING) MODEL #9030

K902299 · CBP

Anesthesiology · 157d

Cleared Aug 22, 1990

ORAL-NASAL MASK RESUSCITATION AND ANESTHETIC GAS

K902298 · BSJ

Anesthesiology · 92d

Cleared Jul 21, 1988

RESCUE MASK & CPR VALVE FOR MOUTH-TO-MASK TYPE CPR

Rondex Products, Inc. - FDA 510(k) Cleared Devices

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