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FDA 510(k) Application Details - K000974
Device Classification Name
Curette, Suction, Endometrial (And Accessories)
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510(K) Number
K000974
Device Name
Curette, Suction, Endometrial (And Accessories)
Applicant
UTAH MEDICAL PRODUCTS, INC.
7043 SOUTH 300 WEST
MIDVALE, UT 84047-1048 US
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Contact
KEVIN L CORNWELL
Other 510(k) Applications for this Contact
Regulation Number
884.1175
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Classification Product Code
HHK
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More FDA Info for this Product Code
Date Received
03/27/2000
Decision Date
05/23/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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