Duns Number:333710619
Catalog Number
PM/PC
Brand Name
ELECTROmatic PM/PC
Version/Model Number
1.011.1900
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K163317
Product Code
EBW
Product Code Name
Controller, foot, handpiece and cord
Public Device Record Key
3d6aa3ad-9378-48cc-b29c-953b76d0ebff
Public Version Date
November 08, 2021
Public Version Number
3
DI Record Publish Date
October 07, 2019
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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 194 |
2 | A medical device with a moderate to high risk that requires special controls. | 153 |