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FDA 510(k) Application Details - K963924
Device Classification Name
Nebulizer (Direct Patient Interface)
More FDA Info for this Device
510(K) Number
K963924
Device Name
Nebulizer (Direct Patient Interface)
Applicant
PARI HOLDING CO.
7493 WHITEPINE RD.
RICHMOND, VA 23237 US
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Contact
MIGUEL A ARRIZON
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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
09/30/1996
Decision Date
12/10/1996
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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