Duns Number:201276334
Device Description: Wrap, 81 X 60, Level 2, single ply
Catalog Number
084B-ON
Brand Name
Lac-Mac
Version/Model Number
084B-ON
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K102864
Product Code
FRG
Product Code Name
Wrap, Sterilization
Public Device Record Key
44cc1d87-2b51-448d-b014-1123cd5c8f43
Public Version Date
July 28, 2020
Public Version Number
6
DI Record Publish Date
September 22, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 216 |