510(k) K233652

Contour Hand/Wrist (Q7000232) by Quality Electrodynamics — Product Code MOS

K233652 is an FDA 510(k) premarket notification submitted by Quality Electrodynamics for the device "Contour Hand/Wrist (Q7000232)". The FDA issued a decision of Substantially Equivalent on February 16, 2024. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Quality Electrodynamics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 2024
Date Received
November 14, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Coil, Magnetic Resonance, Specialty
Device Class
Class II
Regulation Number
892.1000
Review Panel
RA
Submission Type