# K024011: Siss Reprocessed Hot Biopsy Forceps, Laparoscopic, Endoscopic and Electrosurgical Surgical Instruments and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Instruments Service and Savings, Inc.
- Decided: Dec 19, 2002 after 15 days
- Product code: NLU (Forceps, Biopsy, Electric, 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Microvasive/Boston Scientific 1550: named in the summary without a submission number
- (no number) Wilson-Cook HDS-2.5-230: named in the summary without a submission number
- (no number) Ballard Medical 60110: named in the summary without a submission number

## Indications for use
The MediSISS Reprocessed Hot Biopsy Forceps and accessories are intended to be used endoscopically to obtain tissue specimens, remove polyps and cauterize tissue.

Source page: https://510kreport.com/device/K024011
Methodology: https://510kreport.com/methodology