Atlas FDA

BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S)

FDA 510(k) clearance K103345 · decided 2011-02-11

Clearance details

K-number
K103345
Device name
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S)
Applicant
Breathe Technologies, Inc.
Decision
Substantially Equivalent
Date received
2010-11-15
Decision date
2011-02-11
Days to decision
88 days
Clearance type
Traditional
Product code
ONZ
Device class
2
Regulation number
868.5895
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
San Ramon, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
TAV System (K152664)New Aera, Inc.2016-12-02
BREATHE NIOV VENTILATION SYSTEM (K131562)Breathe Technologies2014-03-06
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S) (K102525)Breathe Technologies, Inc.2010-12-02
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES BT-V2S (K100528)Breathe Technologies, Inc.2010-04-23
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (K082982)Breathe Technologies, Inc.2009-07-20

Recalls involving this device

No recalls on record reference this clearance.