# K213824: Sonopet iQ Ultrasonic Aspirator System

- Pathway: 510(k) (Special)
- Applicant: Stryker Corporation
- Decided: Feb 3, 2022 after 57 days
- Product code: LFL (Instrument, Ultrasonic Surgical)
- Device class: U
- 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 K190070 (2019). 1 ancestor in all.
2 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)
- K190070: Sonopet iQ Ultrasonic Aspirator System, Stryker Corporation (2019) Summary page 4.

## Most influential descendants
- K243930: Sonopet iQ Ultrasonic Aspirator System (5500-050-000) (2025), 0 descendants of its own
- K223770: Sonopet 1Q 3 7cm 1Q Large (2023), 0 descendants of its own

## Indications for use
The Sonopet iQ Ultrasonic Aspirator System is indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft tissue and hard tissue is desirable, including Neurosurgery, Gastrointestinal and affiliated Organ surgery, Urological surgery, Plastic and Reconstructive surgery, General surgery, Orthopedic surgery, Gynecological surgery, Thoracic surgery, Laparoscopic surgery, and Thoracoscopic surgery. CONTRAINDICATION: This ultrasonic surgical aspirator device is not indicated for and should not be used for the fragmentation, emulsification, and aspiration of uterine fibroids.

Source page: https://510kreport.com/device/K213824
Methodology: https://510kreport.com/methodology