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FDA 510(k) Application Details - K972528
Device Classification Name
Stretcher, Wheeled
More FDA Info for this Device
510(K) Number
K972528
Device Name
Stretcher, Wheeled
Applicant
DYNA CORP.
6300 YARROW DR.
CARLSBAD, CA 92009-1597 US
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Contact
HENRY C PERRY
Other 510(k) Applications for this Contact
Regulation Number
880.6910
More FDA Info for this Regulation Number
Classification Product Code
FPO
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More FDA Info for this Product Code
Date Received
07/07/1997
Decision Date
07/28/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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