Atlas FDA

Pivot Breath Sensor

FDA 510(k) clearance K201206 · decided 2021-06-30

Clearance details

K-number
K201206
Device name
Pivot Breath Sensor
Applicant
Carrot, Inc.
Decision
Substantially Equivalent
Date received
2020-05-04
Decision date
2021-06-30
Days to decision
422 days
Clearance type
Traditional
Product code
CCJ
Device class
2
Regulation number
868.1430
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Redwood City, CA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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Carbon Monoxide Breath Sensor System (COBSS) (K171408)Carrot Sense, Inc.2017-09-29
CoSense ETCO Monitor (K151107)Capnia, Inc.2015-07-22
COSENSE CO MONITOR (K130036)Capnia, Inc.2014-01-14
COSENSE (K121768)Capnia, Inc.2012-10-31
EC50 MICRO+ SMOKERLYZER (K082315)Bedfont Scientific, Ltd.2010-02-01
TABATABA COTESTER (K080278)Fim Medical2008-11-28
EC50 TOXCO+ BREATH CARBON MONOXIDE MONITOR (K070259)Bedfont Scientific, Ltd.2008-02-21
PICO SMOKERLYZER, MODEL EC-50 (K000962)Bedfont Scientific, Ltd.2000-04-20

Recalls involving this device

No recalls on record reference this clearance.