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

VITAL SYNC MODEL 5000 SERIES

K Number: K093422 · Decision Apr 29, 2010
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
12
Review Days
177

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Basic Information

Device Name
VITAL SYNC MODEL 5000 SERIES
K Number
K093422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somanetics Corp.
Date Received
November 3, 2009
Decision Date
April 29, 2010
Product Code
MWI
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
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Similar 510(k) Clearances

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Other Clearances by Somanetics Corp.

K Number Device Name
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
K051274 INVOS SYSTEM
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. →