Duns Number:055363428
Device Description: Defibrillator ,MAIN ASSY, PS SERIES, LCD, NO VOICE RCDG, JAPANESE
Catalog Number
-
Brand Name
AED PLUS
Version/Model Number
20000000100011360
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
K120406
Product Code
MKJ
Product Code Name
Automated external defibrillators (non-wearable)
Public Device Record Key
f2e48c6e-49ca-4ec5-b8e5-41328b686dcf
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
December 22, 2014
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 | 10 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1473 |
| 3 | A medical device with high risk that requires premarket approval | 1032 |