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FDA 510(k) Application Details - K961848
Device Classification Name
Stethoscope, Electronic
More FDA Info for this Device
510(K) Number
K961848
Device Name
Stethoscope, Electronic
Applicant
MINNESOTA MINING AND MFG. CO.
3M CENTER, BUILDING 275-3E-08
P.O. BOX 33275
ST. PAUL, MN 55133-3275 US
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LINDA JONSEN
Other 510(k) Applications for this Contact
Regulation Number
870.1875
More FDA Info for this Regulation Number
Classification Product Code
DQD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/13/1996
Decision Date
09/26/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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