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FDA 510(k) Application Details - K992322
Device Classification Name
Ventilatory Effort Recorder
More FDA Info for this Device
510(K) Number
K992322
Device Name
Ventilatory Effort Recorder
Applicant
SNAP LABORATORIES, L.L.C.
3633 WEST LAKE AVE., SUITE 406
GLENVIEW, IL 60025 US
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Contact
GIL RAVIV
Other 510(k) Applications for this Contact
Regulation Number
868.2375
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Classification Product Code
MNR
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More FDA Info for this Product Code
Date Received
07/12/1999
Decision Date
02/02/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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