510(k) K890235

DRESSING SCISSORS by Kinetic Medical Products — Product Code LRW

K890235 is an FDA 510(k) premarket notification submitted by Kinetic Medical Products for the device "DRESSING SCISSORS". The FDA issued a decision of Substantially Equivalent on February 3, 1989. The device falls under product code LRW (Scissors, General, Surgical), a Class I device regulated under 21 CFR 878.4800. Kinetic Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1989
Date Received
January 18, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scissors, General, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type