Medical Device
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LMCClass II

Camera, Multi Format, Radiological

21 CFR 892.2040 / Radiology

LMC is the FDA product code for Camera, Multi Format, Radiological, a class II device type, regulated under 21 CFR 892.2040. As of , FDA records hold 121 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
LMC
Device name
Camera, Multi Format, Radiological
Regulation
21 CFR 892.2040
Device class
Class II
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
121
Ingested recalls
3

Clearances, product code LMC

By decision year
121 clearances under product code LMC with a decision year between 1984 and 2014, 1995 the highest year at 12.
Show the numbers
510(k) clearances under FDA product code LMC by decision year
YearClearances
19843
19851
19867
19874
19882
19895
199011
19917
199210
19937
19943
199512
19965
19978
19993
20001
20016
20024
20034
20046
20051
20063
20071
20081
20093
20111
20142

Applicants with the most clearances

Product code LMC

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 18 companies shown, in name order