Catalog Number

DYNJAAC400PM

Brand Name

Medline

Version/Model Number

DYNJAAC400PM

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

K111282

Product Code

FLL

Product Code Name

Thermometer, electronic, clinical

Public Device Record Key

4dcdfb1a-4157-46d2-87b1-2fea3529abdb

Public Version Date

August 05, 2019

Public Version Number

4

DI Record Publish Date

October 14, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-