510(k) K853856

EXTERNAL UTERINE CONTRACTION MONITOR-TOKODYNAMOMET by Aequitron Medical, Inc. — Product Code HFM

K853856 is an FDA 510(k) premarket notification submitted by Aequitron Medical, Inc. for the device "EXTERNAL UTERINE CONTRACTION MONITOR-TOKODYNAMOMET". The FDA issued a decision of Substantially Equivalent on March 12, 1986. The device falls under product code HFM (Monitor, Uterine Contraction, External (For Use In Clinic)), a Class II device regulated under 21 CFR 884.2720. Aequitron Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 12, 1986
Date Received
September 16, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Uterine Contraction, External (For Use In Clinic)
Device Class
Class II
Regulation Number
884.2720
Review Panel
OB
Submission Type