# K992026: Soring GMBH, Sonoca 300

- Pathway: 510(k) (Traditional)
- Applicant: Soring GmbH Medizintechnik
- Decided: Sep 23, 1999 after 99 days
- Product code: BTA (Pump, Portable, Aspiration (Manual Or Powered))
- Device class: 2
- Regulation: 21 CFR 878.4780
- 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 K942095 (1994). 1 ancestor in all.
11 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942095: Sonoca Iii, Holl Meditronics, Inc. (1994) Summary page 1.

## Most influential descendants
- K012753: Soring GMBH Sonoca 180/190 (2001), 6 descendants of its own
- K062544: AR1000 Ultrasonic Wound Therapy System (2007), 5 descendants of its own
- K052183: Soring GMBH Sonoca Lipo (2005), 3 descendants of its own
- K112782: Misonix Sonicone (R) Ultrasonic Wound Care System and Accessories (2011), 2 descendants of its own
- K092066: Phaser Lipoplasty System (Dur-01), Phaser Disposable Kit (Dis-01), Phaser Waste Collection Kit (Was-01), Phaser Cannulae (2010), 2 descendants of its own

## Indications for use
The SONOCA 300 is an instrument intended for selected ultrasound dissection, fragmenting, emulsifying, and aspiration of human tissue and adjunctive irrigation and suction at the operation site during multi-medical discipline surgery including: General Surgery, NE, PED, Thoracic, UR, and GI modalities but not including CV, Ent, Ortho or suction Lipectomy.

Source page: https://510kreport.com/device/K992026
Methodology: https://510kreport.com/methodology