Catalog Number

-

Brand Name

LOGIQ

Version/Model Number

P8 R4.5

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K214039

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

da838b76-67a6-4542-a539-9fa98e668068

Public Version Date

April 05, 2022

Public Version Number

1

DI Record Publish Date

March 28, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-