Catalog Number

8888501023

Brand Name

Argyle

Version/Model Number

8888501023

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

GCX

Product Code Name

APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

Public Device Record Key

a7e826b0-078e-4285-ae45-b72716c92631

Public Version Date

February 15, 2019

Public Version Number

5

DI Record Publish Date

May 24, 2017

Package DI Number

20884521517636

Quantity per Package

50

Contains DI Package

10884521517639

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE