Medical Device Manufacturer · US , Mchenry , IL

Elscint, Inc. - FDA 510(k) Cleared Devices

94 submissions · 94 cleared · Since 1981

Total

Cleared

Denied

Elscint, Inc. has 94 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 94 cleared submissions from 1981 to 1998.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Elscint, Inc.

94 devices

1-12 of 94

Cleared Dec 11, 1998

ADVANCED AUTOMATIC DETECTOR SELECTION OPTION FOR GLORY

K983313 · IZH

Radiology · 81d

Cleared Sep 02, 1998

VOLUMAX CT IMAGING SYSTEM

GYREX 2T PRESTIGE, GYREX PRIMA ITG, GYREX PRIVILEGE, GYREX V-EP

K980306 · LNH

Radiology · 65d

Cleared Mar 04, 1998

GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA...

K974614 · LNH

Radiology · 83d

Cleared Sep 15, 1997

2T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)

GYREX 2T PRESTIGE MODEL NO. 100-6321-0107 AND GYREX PRIVILEGE MODEL NO....

K965044 · LNH

Radiology · 185d

Cleared May 29, 1997

CARDIAC SCORING FOR CT SCANNERS

VOLMETRIC COINCIDENCE DETECTION SYSTEM

K962100 · KPS

Radiology · 225d

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Elscint, Inc. - FDA 510(k) Cleared Devices

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