Catalog Number

-

Brand Name

n.a.

Version/Model Number

26201HL

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

K943700

Product Code

EOQ

Product Code Name

Bronchoscope (flexible or rigid)

Public Device Record Key

efa54971-b803-437e-bf47-36045c737b5b

Public Version Date

January 08, 2021

Public Version Number

2

DI Record Publish Date

February 23, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-