# K960400: Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line Instruments/Diamond-Port (Access Parts)

- Pathway: 510(k) (Traditional)
- Applicant: Snowden-Pencer
- Decided: Mar 12, 1996 after 43 days
- Product code: FBM (Cannula And Trocar, Suprapubic, Non-Disposable)
- Device class: 1
- Regulation: 21 CFR 876.5090
- 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 K930667 (1994). 2 ancestors in all.
273 later devices descend from it; 4 cite it directly.
1 of 276 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K930666: Reusable Laparoscopic Instruments W/ Electrocautery, Snowden-Pencer (1994) Summary page 1.
- K930667: Reusable Laparoscopic Instruments, Snowden-Pencer (1994) Summary page 1.

## Most influential descendants
- K990144: Intuitive Surgical Endoscopic Instruments, Intuitive Surgical Endoscopic Instrument Control System (2000), 269 descendants of its own
- K022574: Intuitive Surgical Endoscopic Instrument Control System & Endoscopic Instruments, Model DA Vinci Isi 1000/1200 (2002), 260 descendants of its own
- K021036: Intuitive Surgical DA Vinci Surgical System, Model IS1000 (2002), 260 descendants of its own
- K040237: Intuitive Surgical DA Vinci Endoscopic Instrument Control System and Endoscopic Instruments (2004), 258 descendants of its own
- K013416: Intuitive Surgical Endowrist Endoscopic Instrument Family (2002), 254 descendants of its own

## Indications for use
Various endoscopic surgical instruments for use in minimally invasive cardiac procedures including single bypass and multiple bypass (coronary artery bypass grafting (CABG) procedures), and saphenous vein harvesting,

Source page: https://510kreport.com/device/K960400
Methodology: https://510kreport.com/methodology