510(k) K925560

ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES by Zinnanti Surgical Instruments, Inc. — Product Code HGI

K925560 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES". The FDA issued a decision of Substantially Equivalent on August 30, 1994. The device falls under product code HGI (Electrocautery, Gynecologic (And Accessories)), a Class II device regulated under 21 CFR 884.4120. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1994
Date Received
November 3, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrocautery, Gynecologic (And Accessories)
Device Class
Class II
Regulation Number
884.4120
Review Panel
OB
Submission Type