Duns Number:054318779
Catalog Number
-
Brand Name
10 Series Plus Wrist Blood Pressure Monitor
Version/Model Number
BP653
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K123498,K123498
Product Code
DXN
Product Code Name
System, Measurement, Blood-Pressure, Non-Invasive
Public Device Record Key
9919a538-defa-4903-a1b1-dbc98eb36fd9
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
September 16, 2016
Package DI Number
10073796266537
Quantity per Package
12
Contains DI Package
00073796266530
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 5 |
2 | A medical device with a moderate to high risk that requires special controls. | 48 |