Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Product codes
NMD
Product code NMD
Device name
Oximeter, Tissue Saturation, Reprocessed
Medical specialty
Cardiovascular
Device class
2
Regulation number
870.2700
Review panel
CV
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K111007
MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE
Midwest Reprocessing Center, LLC
2011-06-08
K100523
ADULT CEREBRAL-SOMATIC OXIMETRY SENSOR, PEDIATRIC CEREBRAL-SOMATIC OXIMETRY SENSOR MODEL HHS-SAFB-SM, HHS-SPFB-USA
Hygia Health Services, Inc.
2010-05-04
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
05415067028709
BurstDRā¢
ST. JUDE MEDICAL, INC.
2018-03-15
10817357022190
Somanetics
HYGIA HEALTH SERVICES, INC.
2017-02-04
30817357022194
Somanetics
HYGIA HEALTH SERVICES, INC.
2017-02-04
10817357020547
Somanetics
HYGIA HEALTH SERVICES, INC.
2016-09-22
30817357020541
Somanetics
HYGIA HEALTH SERVICES, INC.
2016-09-22