# K232808 (us_fda)

FDA 510(k) K232808 for Butterfly iQ3 Ultrasound System (also covers iQ/iQ+). Portable handheld POCUS. Original iQ cleared 2018.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K232808
- Filing date: 2023-01-01
- Decision date: 2023-01-01
- Verification posture: verified

## Applicant

- [Butterfly Network](/companies/butterfly-network.md)

## Covered models (1)

- [Butterfly iQ+](/models/butterfly-iq-plus.md)

## Sources (1)

- [https://www.accessdata.fda.gov/cdrh_docs/pdf23/K232808.pdf](https://www.accessdata.fda.gov/cdrh_docs/pdf23/K232808.pdf)

_Canonical URL: /regulatory-filings/butterfly-iq-plus-fda-510k-k232808. HTML version: [/regulatory-filings/butterfly-iq-plus-fda-510k-k232808](/regulatory-filings/butterfly-iq-plus-fda-510k-k232808)._