Catalog Number

117899

Brand Name

Bore Gauge TruSystem 7500 US

Version/Model Number

01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K133506

Product Code

MOI

Product Code Name

System, Test, Immunological, Antigen, Tumor

Public Device Record Key

6b2b14c6-7ff8-47dc-b291-e752d99971c0

Public Version Date

March 05, 2020

Public Version Number

4

DI Record Publish Date

September 06, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-