Catalog Number

-

Brand Name

PENTAX

Version/Model Number

KW3122S

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K850020,K850020

Product Code

FDS

Product Code Name

Gastroscope and accessories, flexible/rigid

Public Device Record Key

116cd864-c393-4fc9-84a7-61b7f82fb6e9

Public Version Date

July 12, 2019

Public Version Number

5

DI Record Publish Date

April 07, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-