# K932456: Jarit Surgical Instruments

- Pathway: 510(k) (Traditional)
- Applicant: J. Jamner Surgical Instruments, Inc.
- Decided: Apr 21, 1994 after 335 days
- Product code: KNF (Coagulator-Cutter, Endoscopic, Unipolar (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.4160
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K120012: Integra Jarit Video Assisted Thoracic Surgery Instruments (2012), 1 descendant of its own
- K152400: General & Plastic Surgery Instruments (2016), 0 descendants of its own
- K103726: Jarit Take-Apart Endoscopic Instruments (2012), 0 descendants of its own

## Recalls of this device
- Feb 12, 2013 · Class II · Z-0886-2013: Addendum to the Instructions for Use. The addendum emphasizes the warnings and precautions already contained in the device's IFU and also provides additional warnings and precautions that are applicab

Source page: https://510kreport.com/device/K932456
Methodology: https://510kreport.com/methodology