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

GYREX 2T-PRESTIGE

K Number: K970005 · Decision Mar 28, 1997
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
9
Applicant Total
94
Review Days
85

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Basic Information

Device Name
GYREX 2T-PRESTIGE
K Number
K970005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elscint, Inc.
Date Received
January 2, 1997
Decision Date
March 28, 1997
Product Code
LNI
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
LNI System, Nuclear Magnetic Resonance Spectroscopic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LNI), ordered by most recent decision date.

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Other Clearances by Elscint, Inc.

K Number Device Name
K983313 ADVANCED AUTOMATIC DETECTOR SELECTION OPTION FOR GLORY
K982060 VOLUMAX CT IMAGING SYSTEM
K974344 CT SCOPE
K980306 GYREX 2T PRESTIGE, GYREX PRIMA ITG, GYREX PRIVILEGE, GYREX V-EP
K974614 GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA 1TG 100-6250-0102
K972592 2T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)
K970680 GLORY
K965044 GYREX 2T PRESTIGE MODEL NO. 100-6321-0107 AND GYREX PRIVILEGE MODEL NO. 100-6326-0102
K970980 CARDIAC SCORING FOR CT SCANNERS
K964583 XRT-7.0
Search all 94 clearances from Elscint, Inc. →