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FDA 510(k) Application Details - K072026
Device Classification Name
Stethoscope, Electronic
More FDA Info for this Device
510(K) Number
K072026
Device Name
Stethoscope, Electronic
Applicant
RNK PRODUCTS, INC.
12700 DIAMOND DRIVE
BURNSVILLE, MN 55337 US
Other 510(k) Applications for this Company
Contact
CHARLES R ABBRUSCATO
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
07/24/2007
Decision Date
10/26/2007
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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