Catalog Number
-
Brand Name
Mon-a-Therm
Version/Model Number
502-0411A
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"
Yes
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
K895875,K895875
Product Code
FLL
Product Code Name
Thermometer, electronic, clinical
Public Device Record Key
3c2f9504-e71d-4b2b-82cd-c9cdd430249a
Public Version Date
July 05, 2022
Public Version Number
2
DI Record Publish Date
February 21, 2019
Package DI Number
10884521706439
Quantity per Package
40
Contains DI Package
10884521169319
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 132 |
2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
3 | A medical device with high risk that requires premarket approval | 202 |
U | Unclassified | 40 |