Duns Number:188354831
Device Description: 1. 20x12-well ANCA Neutrophil substrate slides (formalin-fixed)2. 1x 1mL pANCA Positive Co 1. 20x12-well ANCA Neutrophil substrate slides (formalin-fixed)2. 1x 1mL pANCA Positive Control (prediluted) 3. 1x 1mL cANCA Positive Control (prediluted) 4. 1x 1mL ANA Positive Control (prediluted) 5. 1x 1mL IFA System Negative Control6. 1x 15mL anti Human IgG AFF Fluorescein with Evans Blue7. 2x 25mL PBS II Concentrate (40x)8. 1x 3mL 1% Evans Blue 9. 1x 10mL Mounting Medium10. 1x 20 Coverslips11. 1x Instruction leaflet
Catalog Number
-
Brand Name
NOVA Lite® ANCA Formalin Kit
Version/Model Number
708297
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
K965133
Product Code
MOB
Product Code Name
Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
Public Device Record Key
6ad0b127-37bf-40e1-bf67-d38e04adc085
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
August 31, 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 | 36 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 215 |