Duns Number:933442068
Device Description: Double-Sided Rasp
Catalog Number
1760-7039
Brand Name
Pisces-SA
Version/Model Number
1760-7039
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
-
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
K213935
Product Code
HTR
Product Code Name
Rasp
Public Device Record Key
8f9f0acc-596f-4f48-9f67-87a62ca6fff1
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
May 24, 2022
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 | 305 |
2 | A medical device with a moderate to high risk that requires special controls. | 918 |