Needle Holders & Access for Lapar Surg-Ob/Gyn Use

FDA 510(k) K926021 · Zinnanti Surgical Instruments, Inc.

Substantially Equivalent

510(k) numberK926021

Submission

Device name
Needle Holders & Access for Lapar Surg-Ob/Gyn Use
Applicant
Zinnanti Surgical Instruments, Inc.
Chatsworth, CA, US
Received
November 30, 1992
Decision date
April 7, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HET – Laparoscope, Gynecologic (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1720
Specialty
Obstetrics/Gynecology

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More from 270surgical , Ltd.

510(k)DeviceDecision
K925501Nylon Coated SpeculaHIB · Traditional 06/13/1997SE
K941458Uterine Manipulator/Injector with SpringLKF · Traditional 01/25/1995SE
K941457Uterine Injector with SpringLKF · Traditional 01/24/1995SE
K925560Zsi Loop, Zsi Ball & Zsi Needle ElectrodesHGI · Traditional 08/30/1994SE
K925960Forceps for Laparoscopic Surgery OB/GYN UseHFI · Traditional 06/07/1994SE
K925957Scissors for Laparoscopic Surgery OB/GYN UseHFI · Traditional 06/07/1994SE
K925958Scissor for Laparoscopic Surgery Gu UseGCJ · Traditional 03/24/1994SE
K926181Zsi Laparoscopes-General & Plastic SurgeryGCJ · Traditional 12/17/1993SE
K926016Needle Holders & Access for Lapar Surg-Gu UseGCJ · Traditional 11/12/1993SE
K925959Forceps for Laparoscopic Surgery Gu UseGCJ · Traditional 11/12/1993SE

Questions and answers

When was Needle Holders & Access for Lapar Surg-Ob/Gyn Use cleared by the FDA?

Needle Holders & Access for Lapar Surg-Ob/Gyn Use (K926021) received a 510(k) decision of Substantially Equivalent on April 7, 1994, 493 days after the submission was received.

What is the product code of K926021?

The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.