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

CORRESTORE PATCH SYSTEM

K Number: K040162 · Decision Mar 16, 2004
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
89
Applicant Total
12
Review Days
50

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Basic Information

Device Name
CORRESTORE PATCH SYSTEM
K Number
K040162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3470
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somanetics Corp.
Date Received
January 26, 2004
Decision Date
March 16, 2004
Product Code
DXZ
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
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXZ), ordered by most recent decision date.

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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
K051274 INVOS 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. →