Duns Number:006261481
Device Description: Y-ADAPTER AC4001M PITON TJM 5PK
Catalog Number
-
Brand Name
PITON™ Y-ADAPTOR
Version/Model Number
AC4001M
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
K940063,K940063
Product Code
LIT
Product Code Name
Catheter, angioplasty, peripheral, transluminal
Public Device Record Key
af003141-53cf-4441-b08b-7f14c365dcc1
Public Version Date
October 23, 2019
Public Version Number
4
DI Record Publish Date
July 04, 2016
Package DI Number
20643169002931
Quantity per Package
5
Contains DI Package
00643169002937
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
PK
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |