Duns Number:482163628
Device Description: Procedure Pack for Cataract Surgery
Catalog Number
510.700.117
Brand Name
Procedure Pack Z8
Version/Model Number
Cataract
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
K150323,K150323
Product Code
OOE
Product Code Name
Ophthalmic Femtosecond Laser
Public Device Record Key
a16dc79d-a5c5-45e9-9eb2-c94058a7248d
Public Version Date
November 08, 2019
Public Version Number
2
DI Record Publish Date
September 14, 2018
Package DI Number
07640167751068
Quantity per Package
10
Contains DI Package
07640167750528
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 20 |
2 | A medical device with a moderate to high risk that requires special controls. | 23 |