Catalog Number

ENDOPROBE 30 DEG STEP, 23G

Brand Name

ACC. PROBE, ENDO, 30 DEG STEP, 23G

Version/Model Number

A877000

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K050807,K050807

Product Code

HQF

Product Code Name

Laser, Ophthalmic

Public Device Record Key

0fa99a32-b731-475d-9ecf-457c383f6c8d

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 21, 2017

Package DI Number

09342395000953

Quantity per Package

10

Contains DI Package

09342395001929

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX