Duns Number:002111896
Device Description: Radiolucent Foam Electrodes60/pouch, 600 /case
Catalog Number
LMC 202
Brand Name
L.M.C Associates, Inc
Version/Model Number
LMC 202
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DRX
Product Code Name
Electrode, Electrocardiograph
Public Device Record Key
2efda4b1-05f7-4be2-aeb9-dbe1522a0a8c
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
April 14, 2017
Package DI Number
20813150022457
Quantity per Package
10
Contains DI Package
10813150022450
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 161 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 269 |
| 3 | A medical device with high risk that requires premarket approval | 1 |