DuoFLEX Coil Suite— 510(k) K173290
Substantially EquivalentMr Instruments, Inc.
FDA 510(k) clearance K173290 for DuoFLEX Coil Suite, Substantially Equivalent on 2017-11-28. Applicant: Mr Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Mr Instruments, Inc.
- 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
- Minnetonka, MN, US
Recent devices under product code MOS
view all- K262330 — dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil 7ch 1.5TdS Sentinelle Breast 16ch 1.5TdS Sentinelle Breast 16ch 3.0T
- K262294 — dS FootAnkle 16Ch 1.5T +5 more
- K260947 — 0.55T 12Ch Breast Coil
- K252587 — HD 8Ch Wrist Array
- K252876 — GEM Flex Coil 16-L Array, 3.0T Receive Only +2 more
More clearances from Mr Instruments, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.