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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K093853

SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES · Nonin Medical, Inc. · decided 2010-06-04 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Nonin7000ANONIN MEDICAL, INC.DQA00849686072518
Nonin3013 CHNONIN MEDICAL, INC.DQA00833166001242
Nonin6100CPNONIN MEDICAL, INC.DQA00849686073324
Nonin7000PNONIN MEDICAL, INC.DQA00849686072501
Nonin3013FHNONIN MEDICAL, INC.DQA00833166001259
Nonin7000INONIN MEDICAL, INC.DQA00849686072495
Nonin6100CNNONIN MEDICAL, INC.DQA00849686073300
Nonin7000NNONIN MEDICAL, INC.DQA00849686072488
Nonin6000CPNONIN MEDICAL, INC.DQA00849686072549
WristOx2 ® Pulse Oximeter6000CA-WO2NONIN MEDICAL, INC.DQA00849686050943
Nonin6000CANONIN MEDICAL, INC.DQA00849686072556
Nonin6000CNNONIN MEDICAL, INC.DQA00849686072525
Nonin6000CINONIN MEDICAL, INC.DQA00849686072532