# K052104: Ultraclean Handcontrolled Suction Coagulator, Model 130182, 130183, 130184, 130185; Ultraclean Footcontrolled Suction

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Oct 21, 2005 after 79 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K033003 (2004). 1 ancestor in all.
26 later devices descend from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033003: Suction Coagulator, Modern Medical Equipment Mfg., Ltd. (2004) Summary page 1.

## Most influential descendants
- K073616: Fas-Clean Electrosurgical Coated Active Blade (2008), 25 descendants of its own
- K082786: Pulsar Generator, Peak Plasmablade; 4.0, Needle, and Ext Tissue Dissection Devices (2008), 24 descendants of its own
- K093695: Peak Plasmablade 3.OS Tissue Dissection Device (2010), 8 descendants of its own
- K142410: Elliquence Electrodes (2015), 7 descendants of its own
- K160041: Cobbra RF Tissue Dissector (2016), 6 descendants of its own

## Recalls of this device
- Sep 30, 2009 · Not classified · Z-0165-2010: One production lot of Suction Coagulators received ETO sterilization instead of gamma radiation sterilization.

## Indications for use
Single-use electrosurgical accessory used to provide coagulation therapeutic energy to tissue and suction to aspirate blood, coagulum and small bits of tissue debris from the surgical site. The coagulation effect is achieved by the passage of high frequency current through the tissue of interest.

Source page: https://510kreport.com/device/K052104
Methodology: https://510kreport.com/methodology