FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 30

K Number: K060546 · Decision May 26, 2006
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
46
Applicant Total
15
Review Days
86

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Basic Information

Device Name
BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 30
K Number
K060546
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Breas Medical AB
Date Received
March 1, 2006
Decision Date
May 26, 2006
Product Code
MNS
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
MNS Ventilator, Continuous, Non-Life-Supporting

Similar 510(k) Clearances

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

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Other Clearances by Breas Medical AB

K Number Device Name
K242485 EveryWare
K242438 Clearo
K233452 Vivo 45 LS
K240779 Vivo 3
K240778 Vivo 1, Vivo 2
K193586 Vivo 45 LS
K160481 Vivo 60
K090113 BREAS VIVO 40 SYSTEM
K071702 BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40
K063476 BREAS ISLEEP 20I
Search all 15 clearances from Breas Medical AB →