JAM — Scanner, Whole Body, Nuclear Class I

FDA Device Classification

FDA product code JAM covers "Scanner, Whole Body, Nuclear", a Class I medical device regulated under 21 CFR 892.1330. Submissions are reviewed by the Radiology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JAM
Device Class
Class I
Regulation Number
892.1330
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842895siemens gammasonicsWBA - I.R.I.S.August 27, 1984
K841996general electricMAXICAMERA 400T W/BODY CONTOUR TOMOGRAJuly 16, 1984
K770530union carbideCLEON IMAGERApril 5, 1977