Atlas FDA

COOPDECH ENDOBRONCHIAL BLOCKER TUBE, MODELS BBT-A30XXX, BBT-B30XXX

FDA 510(k) clearance K071694 · decided 2008-03-20

Clearance details

K-number
K071694
Device name
COOPDECH ENDOBRONCHIAL BLOCKER TUBE, MODELS BBT-A30XXX, BBT-B30XXX
Applicant
Daiken Medical Co, Ltd.
Decision
Substantially Equivalent
Date received
2007-06-20
Decision date
2008-03-20
Days to decision
274 days
Clearance type
Traditional
Product code
CBI
Device class
2
Regulation number
868.5740
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Tokyo, JP
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
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Recalls involving this device

No recalls on record reference this clearance.