FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INVOS SYSTEM

K Number: K051274 · Decision Nov 4, 2005
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
73
Applicant Total
12
Review Days
171

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Basic Information

Device Name
INVOS SYSTEM
K Number
K051274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somanetics Corp.
Date Received
May 17, 2005
Decision Date
November 4, 2005
Product Code
MUD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUD Oximeter, Tissue Saturation

Similar 510(k) Clearances

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Other Clearances by Somanetics Corp.

K Number Device Name
K093422 VITAL SYNC MODEL 5000 SERIES
K091224 OXYALERT NIRSENSORS, ACCESSORIES FOR INVOS 5100C SYSTEM, MODELS: IS-C AND IS-S
K082327 INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL: 5100C
K080769 INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL 5100C
K040162 CORRESTORE PATCH SYSTEM
K031586 CORRESTORE PATCH SYSTEM
K011487 CORRESTORE PATCH, MODELS 1.5P2, 2P3, 3P4; CORRESTORE SIZER, MODEL CRPS
K001842 ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100
K971628 SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS)
K960614 SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS)
Search all 12 clearances from Somanetics Corp. →