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

Vivo 60

K Number: K160481 · Decision Nov 9, 2016
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
6
Applicant Total
15
Review Days
261

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Vivo 60
K Number
K160481
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
February 22, 2016
Decision Date
November 9, 2016
Product Code
NOU
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
NOU Continuous, Ventilator, Home Use

Similar 510(k) Clearances

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

View all

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
K090113 BREAS VIVO 40 SYSTEM
K071702 BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40
K063476 BREAS ISLEEP 20I
K060657 ISLEEP BY BREAS, MODELS ISLEEP 10, ISLEEP 20.
Search all 15 clearances from Breas Medical AB →