Duns Number:808204957
Device Description: 5 lead ECG patient cable to be used with the Chroma device.
Catalog Number
-
Brand Name
Chroma 5 Lead Patient Cable
Version/Model Number
100605
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
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"
-
For Single-Use
-
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
K083382
Product Code
MWJ
Product Code Name
Electrocardiograph,Ambulatory(Without Analysis)
Public Device Record Key
dbea8215-6b84-4688-b877-b044b7022255
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
January 23, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 32 |