510(k) K023084

MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL by Medical Advances, Inc. — Product Code MOS

K023084 is an FDA 510(k) premarket notification submitted by Medical Advances, Inc. for the device "MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL". The FDA issued a decision of Substantially Equivalent on Dec 16, 2002. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Medical Advances, Inc. has 56 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 16, 2002
Date Received
Sep 17, 2002
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
510(k)

Source: FDA 510(k) database entry for K023084. Report a data issue: hello@regdatalab.com.