510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071702Substantially Equivalent

Breas Vivo Bilevel System, Model Vivo 40

Breas Medical AB, Molnlycke, SE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071702 is the FDA 510(k) clearance record for BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40, a class II device, cleared for Breas Medical AB on under FDA product code MNT (Sv70 Ventilator). FDA records list 16 510(k) clearances for Breas Medical AB, from to . As of , FDA records show no recalls naming K071702.

Clearance record

Decision date
Received
(239 days to decision)
Product code
MNT Continuous, Minimal Ventilatory Support, Facility Use Ventilator
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Breas Medical AB Foretagsvagen 1, Molnlycke, SE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNT

Trailing 12 months
1 clearance under product code MNT in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MNT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260