Atlas FDA

EC50 TOXCO+ BREATH CARBON MONOXIDE MONITOR

FDA 510(k) clearance K070259 · decided 2008-02-21

Clearance details

K-number
K070259
Device name
EC50 TOXCO+ BREATH CARBON MONOXIDE MONITOR
Applicant
Bedfont Scientific, Ltd.
Decision
Substantially Equivalent
Date received
2007-01-26
Decision date
2008-02-21
Days to decision
391 days
Clearance type
Traditional
Product code
CCJ
Device class
2
Regulation number
868.1430
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Crofton, MD, US
Third-party review
Yes
Expedited review
No

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

RecordFirmDate
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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
PICO SMOKERLYZER, MODEL EC-50 (K000962)Bedfont Scientific, Ltd.2000-04-20

Recalls involving this device

No recalls on record reference this clearance.