FDA 510(k) Application Details - K925388

Device Classification Name Filter, Bacterial, Breathing-Circuit

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510(K) Number K925388
Device Name Filter, Bacterial, Breathing-Circuit
Applicant LIFE SHIELD HEALTHCARE PRODUCTS, INC.
15381 STONY CREEK WAY
NOBLESVILLE, IN US
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Contact TIMOTHY D STRUTHERS
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Regulation Number 868.5260

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Classification Product Code CAH
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Date Received 10/26/1992
Decision Date 05/11/1993
Decision SE - Substantially Equivalent
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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