510(k) K851111

RANDALL KIDNEY STONE FORCEPS 817-84 PCS. HALF CURV by The Huxley Instrument Corp. — Product Code KOA

K851111 is an FDA 510(k) premarket notification submitted by The Huxley Instrument Corp. for the device "RANDALL KIDNEY STONE FORCEPS 817-84 PCS. HALF CURV". The FDA issued a decision of Substantially Equivalent on April 3, 1985. The device falls under product code KOA (Surgical Instruments, G-U, Manual (And Accessories)), a Class I device regulated under 21 CFR 876.4730. The Huxley Instrument Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 3, 1985
Date Received
March 19, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Surgical Instruments, G-U, Manual (And Accessories)
Device Class
Class I
Regulation Number
876.4730
Review Panel
GU
Submission Type