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FDA 510(k) Application Details - K970542
Device Classification Name
Nebulizer (Direct Patient Interface)
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510(K) Number
K970542
Device Name
Nebulizer (Direct Patient Interface)
Applicant
BREMED ITALIA, S.R.L.
1337 ROCKWOOD FOREST DR.
ARNOLD, MO 63010 US
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Contact
MARK HEBENSTREIT
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Regulation Number
868.5630
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Classification Product Code
CAF
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More FDA Info for this Product Code
Date Received
02/12/1997
Decision Date
06/24/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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