510(k) K232787
- Device
- ScanNav Anatomy Peripheral Nerve Block
- Applicant
- Intelligent Ultrasound Limited
- 510(k) number
- K232787
- Product code
- QRG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2023-10-06
- Date received
- 2023-09-11
- Regulation
- 868.1980
- Classification name
- Ultrasound Guided Nerve Block Assist
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Bhaskar Chikkanna
- Address
- Floor 6a, Hodge House, 114-116 St. Mary St. Cardiff GB CF101DY CF101DY
FDA Registration Numbers#
- 3042158826