FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ECLIPSE

K Number: K030981 · Decision Jun 24, 2003
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
170
Review Days
88

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Basic Information

Device Name
ECLIPSE
K Number
K030981
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems, Inc.
Date Received
March 28, 2003
Decision Date
June 24, 2003
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

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