Duns Number:176458115
Device Description: Triple slide patient take home version of a rapid test for the qualitative detection of oc Triple slide patient take home version of a rapid test for the qualitative detection of occult blood in stool specimens.
Catalog Number
-
Brand Name
COMPLIANCE GOLD FECAL OCCULT BLOOD TEST – ER, 50 TRI-SLIDES
Version/Model Number
74250
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
-
Product Code
KHE
Product Code Name
Reagent, Occult Blood
Public Device Record Key
b6670d34-267e-4754-8661-b3cab61e9660
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
May 17, 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 | 12 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 22 |