510(k) K211140

Device
Reprocessed Masimo Pulse Oximeter (1859 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (1860 Pediatric O2 Transducer), Reprocessed Masimo Pulse Oximeter (1861 Infant O2 Transducer), Reprocessed Masimo Pulse Oximeter (1862 Adult O2 Transducer
Applicant
Stryker Sustainability Solutions
510(k) number
K211140
Product code
DQA
Decision
Substantially Equivalent (SESE)
Decision date
2022-03-08
Date received
2021-04-16
Regulation
870.2700
Classification name
Oximeter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Moira Barton-Varty
Address
1810 W Dr.Ake Dr. Tempe AZ US 85283 85283

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code DQA#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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