Catalog Number

-

Brand Name

TMSi

Version/Model Number

8

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K060374

Product Code

GWL

Product Code Name

AMPLIFIER, PHYSIOLOGICAL SIGNAL

Public Device Record Key

70771747-92c3-4c42-a066-6df7b65c5b07

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 16, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-