FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L, 10LB, H10L, H5C10L) and SonoFinder Wireless Probe Type Ultrasound Scanner (Model: SF14L25)
K Number: K220169
·
Decision Oct 11, 2022
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
11
Review Days
264
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L, 10LB, H10L, H5C10L) and SonoFinder Wireless Probe Type Ultrasound Scanner (Model: SF14L25)
- K Number
- K220169
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1550
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bionet Co., Ltd.
- Date Received
- January 20, 2022
- Decision Date
- October 11, 2022
- Product Code
- IYN
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| IYN | System, Imaging, Pulsed Doppler, Ultrasonic | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IYN), ordered by most recent decision date.
ACUSON Sequoia Diagnostic Ultrasound System;ACUSON Sequoia Select Diagnostic Ultrasound System;ACUSON Origin Diagnostic Ultrasound System;ACUSON Origin ICE Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
ES-Series
FDA 510(k)
FDA Class 2
·Radiology
EPIQ Series Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
FDA 510(k)
FDA Class 2
·Radiology
LOGIQ e
FDA 510(k)
FDA Class 2
·Radiology
SonoPort Series Digital Color Doppler Ultrasound System (SonoPort 1, SonoPort 1 Exp, SonoPort 1 Pro, SonoPort 1 Elite, SonoPort 1 Plus, SonoPort 2, SonoPort 2 Exp, SonoPort 2 Pro, SonoPort 2 Elite, SonoPort 2 Plus, SonoPort 3, SonoPort 3 Exp, SonoPort 3 Pro, SonoPort 3 Elite, SonoPort 3 Plus, SonoPort 4, SonoPort 4 Exp, SonoPort 4 Pro, SonoPort 4 Elite, SonoPort 4 Plus, SonoPort 5, SonoPort 5 Exp, SonoPort 5 Pro, SonoPort 5 Elite, SonoPort 5 Plus, SonoPort 6, SonoPort 6 Exp, SonoPort 6
FDA 510(k)
FDA Class 2
·Radiology
Other Clearances by Bionet Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K231160 | Cardio Q50, Cardio Q70 | Dec 15, 2023 | Substantially Equivalent |
| K231150 | Cardio P1 | Nov 9, 2023 | Substantially Equivalent |
| K220535 | Cardio10 | Nov 15, 2022 | Substantially Equivalent |
| K130322 | SPM-300 | Nov 15, 2013 | Substantially Equivalent |
| K113306 | CARDIO 7 | Jul 16, 2012 | Substantially Equivalent |
| K102767 | CARDIO XP | Jun 3, 2011 | Substantially Equivalent |
| K090895 | EKG-PLUS II SOFTWARE | Aug 26, 2009 | Substantially Equivalent |
| K082008 | BIONET BM3PLUS PATIENT MONITOR | Dec 11, 2008 | Substantially Equivalent |
| K043597 | FC 700 FETAL MONITOR | Dec 16, 2005 | Substantially Equivalent |
| K043598 | FC 1400 FETAL MONITOR | Dec 16, 2005 | Substantially Equivalent |