Atlas FDA

JAM

3 FDA 510(k) clearances · Product code

FDA profile

Official device name
Scanner, Whole Body, Nuclear
Device class
Class I (low risk)
Regulation
21 CFR 892.1330
Medical specialty
Radiology
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RecordFirmDate
WBA - I.R.I.S. (K842895)Siemens Gammasonics, Inc.1984-08-27
MAXICAMERA 400T W/BODY CONTOUR TOMOGRA (K841996)General Electric Co.1984-07-16
CLEON IMAGER (K770530)Union Carbide Corp.1977-04-05

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Every clearance here is in the API, with alerts when new ones post.