510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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JAMClass I

Scanner, Whole Body, Nuclear

21 CFR 892.1330 / Radiology
FDA source (opens on fda.gov)

JAM is the FDA product code for Scanner, Whole Body, Nuclear, a class I device type, regulated under 21 CFR 892.1330. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JAM
Device name
Scanner, Whole Body, Nuclear
Regulation
21 CFR 892.1330
Device class
Class I
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code JAM

By decision year
3 clearances under product code JAM with a decision year between 1977 and 1984, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JAM by decision year
YearClearances
19771
19842

Applicants with the most clearances

Product code JAM
Applicants holding the most 510(k) clearances under product code JAM
ApplicantClearances
General Electric Co.1
Siemens Gammasonics, Inc.1
Union Carbide Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code