510(k) K000974

FOWLER ENDOCURETTE, MODEL CUR-XXX by Utah Medical Products, Inc. — Product Code HHK

K000974 is an FDA 510(k) premarket notification submitted by Utah Medical Products, Inc. for the device "FOWLER ENDOCURETTE, MODEL CUR-XXX". The FDA issued a decision of Substantially Equivalent on May 23, 2000. The device falls under product code HHK (Curette, Suction, Endometrial (And Accessories)), a Class II device regulated under 21 CFR 884.1175. Utah Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 23, 2000
Date Received
March 27, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Curette, Suction, Endometrial (And Accessories)
Device Class
Class II
Regulation Number
884.1175
Review Panel
OB
Submission Type