Duns Number:055363428
Device Description: Defibrillator ,MAIN, MANUAL-2, 3/5 LD, STD CONN, AC PWR, CF/STD, DMST, REFURB
Catalog Number
-
Brand Name
R SERIES
Version/Model Number
10001000001030012
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
K990762
Product Code
DPS
Product Code Name
ELECTROCARDIOGRAPH
Public Device Record Key
59fa1727-fc38-43ce-8b11-9d04e1bda512
Public Version Date
December 31, 2019
Public Version Number
4
DI Record Publish Date
October 11, 2016
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 |