8ch Wrist Coil— 510(k) K222325
Substantially EquivalentInvivo Corporation (Business Trade Name: Philips)
FDA 510(k) clearance K222325 for 8ch Wrist Coil, Substantially Equivalent on 2022-08-31. Applicant: Invivo Corporation (Business Trade Name: Philips). Device class: 2.
Clearance details
- Applicant
- Invivo Corporation (Business Trade Name: Philips)
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Florida, FL, US
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More clearances from Invivo Corporation (Business Trade Name: Philips)
view allData sourced from openFDA. This site is unofficial and independent of the FDA.