Duns Number:544332470
Catalog Number
-
Brand Name
simzo
Version/Model Number
HW-F7
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 15, 2021
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
K173048
Product Code
FLL
Product Code Name
Thermometer, Electronic, Clinical
Public Device Record Key
ae0a6fed-63e5-45ba-b243-abfc23cf5fd6
Public Version Date
July 28, 2021
Public Version Number
5
DI Record Publish Date
June 04, 2020
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. | 25 |