Duns Number:830350380
Device Description: CONSOLE 2340000 POWEREASE IPC
Catalog Number
-
Brand Name
POWEREASE™ Instruments
Version/Model Number
2340000
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K111520
Product Code
GWF
Product Code Name
STIMULATOR, ELECTRICAL, EVOKED RESPONSE
Public Device Record Key
54c986e3-25ba-4b1e-a587-d9bf483e4676
Public Version Date
November 22, 2018
Public Version Number
4
DI Record Publish Date
February 13, 2018
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 | 13352 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 26085 |
| 3 | A medical device with high risk that requires premarket approval | 190 |
| U | Unclassified | 75 |