# K134047: Jarit Gynecological Forceps, Miltex Gynecological Forceps, Meisterhand Gynecoloical Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Integra LifeSciences Corporation
- Decided: Apr 11, 2014 after 101 days
- Product code: HCZ (Forceps, Surgical, Gynecological)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K092840 (2009). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092840: Instrumed Forceps Obstetrical/Gynaecological, Instrumed International, Inc. (2009) Summary page 2.
- (no number) Miltex® Gynecological Forceps: named in the summary without a submission number
- (no number) Miniclamps, Stabiliz, Fallopian Tube: named in the summary without a submission number

## Most influential descendants
- K172661: Fetzer Medical Gynecological Forceps (2018), 0 descendants of its own

## Indications for use
Integra® Gynecological Surgical Forceps are hand-held instruments with dual blades that are indicated for pulling, grasping, holding, or compressing tissue during gynecological procedures.

Source page: https://510kreport.com/device/K134047
Methodology: https://510kreport.com/methodology