510(k) K890382

COMPRESSION FORCEPS by Kinetic Medical Products — Product Code HFW

K890382 is an FDA 510(k) premarket notification submitted by Kinetic Medical Products for the device "COMPRESSION FORCEPS". The FDA issued a decision of Substantially Equivalent on February 27, 1989. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530. Kinetic Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 27, 1989
Date Received
January 23, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Clamp, Umbilical
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type