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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Coil, Magnetic Resonance, Specialty
510(k) Number K980157
Device Name PREMIER 7000 CTL SPINE COIL
Applicant
USA INSTRUMENTS, INC.
675-B ALPHA DR.
HIGHLAND HEIGHTS,  OH  44143
Applicant Contact RONY THOMAS
Correspondent
USA INSTRUMENTS, INC.
675-B ALPHA DR.
HIGHLAND HEIGHTS,  OH  44143
Correspondent Contact RONY THOMAS
Regulation Number892.1000
Classification Product Code
MOS  
Date Received01/16/1998
Decision Date 04/13/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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