Atlas FDA

BREATH TRACKER

FDA 510(k) clearance K892942 · decided 1989-06-23

Clearance details

K-number
K892942
Device name
BREATH TRACKER
Applicant
Core-M, Inc.
Decision
Substantially Equivalent
Date received
1989-04-21
Decision date
1989-06-23
Days to decision
63 days
Clearance type
Traditional
Product code
CAP
Device class
2
Regulation number
868.2600
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Brookline, MA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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DISPOSABLE PRESSURE MANOMETER (K140370)Besmed Health Business Corp2014-06-19
GIO DIGITAL PRESSURE GUAGES (K122627)Galemed Corp.2013-08-22
MANOMETER (K122077)Intersurgical, Inc.2013-01-10
VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER (K120118)Ventlab Corp.2012-05-24
VORTRAN AIRWAY PRESSURE MONITOR (VAPM)-ADULT, VORTRAN AIRWAY PRESSURE MONITOR (VAPM)- PEDIATRIC (K103639)Vortran Medical Technology 1, Inc.2011-09-15
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Recalls involving this device

No recalls on record reference this clearance.