Duns Number:122561087
Device Description: BD Veritor™ System For Rapid Detection of Group A Strep Contains: 30 Strep A Devices BD Veritor™ System For Rapid Detection of Group A Strep Contains: 30 Strep A Devices, 30 GAS Reagent 2 in unitized tubes, 30 individually wrapped, sterile throat swabs, one 4 mL dropper bottle GAS Reagent 1, one each of positive and negative control swabs
Catalog Number
256040
Brand Name
BD Veritor™ System For Rapid Detection of Group A Strep - CLIA waived kit
Version/Model Number
256040
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
Yes
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
K122718
Product Code
GTY
Product Code Name
ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.
Public Device Record Key
9ab8ff68-578a-4102-bded-99a2f03ff154
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
May 25, 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 | 611 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 614 |
| 3 | A medical device with high risk that requires premarket approval | 36 |
| U | Unclassified | 4 |