# K030919: Siss, Inc. (D.B.a.Medisiss) Reprocessd Electrosurgical Instruments and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Medisiss
- Decided: Jul 3, 2003 after 101 days
- Product code: NLR (Unit, Electrosurgical, Endoscopic (With Or Without Accessories), Reprocessed)
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K952149 (1995). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K884306: Bicap Ablating Forceps Baf-7, Circon Acmi (1989) Summary page 1.
- K932293: Cabot Medical Bipolar Cutting Forceps, Cabot Medical Corp. (1994) Summary page 1.
- K965176: Pilling Weck 2 Piece Take-Apart Instruments, Pilling Weck Group (1997) Summary page 1.

## Indications for use
The SISS Inc. (d.b.a. MediSISS) Reprocessed electrosurgical instruments have applications in a variety of minimally invasive surgical procedures to manipulate and manage internal soft tissue by grasping, cutting, and/or to facilitate coagulation, transection, resection, mobilization, and dissections of tissue.

Source page: https://510kreport.com/device/K030919
Methodology: https://510kreport.com/methodology