Duns Number:959181160
Device Description: MCA Kit, 5.9 mm OD x 250 mm Length
Catalog Number
MCA-59-250
Brand Name
ClearPoint PURSUIT
Version/Model Number
MCA-59-250
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K181731
Product Code
GWG
Product Code Name
Endoscope, Neurological
Public Device Record Key
8dc2059d-fe6e-40e0-96b2-0a26c0eb3847
Public Version Date
June 27, 2022
Public Version Number
2
DI Record Publish Date
January 22, 2021
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 | 8 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 138 |