Catalog Number

L670-210

Brand Name

Life Support Products

Version/Model Number

L670-210

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"

Yes

For Single-Use

Yes

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

K973106,K973106

Product Code

BTM

Product Code Name

Ventilator, Emergency, Manual (Resuscitator)

Public Device Record Key

cde2825f-dd9b-427a-8694-5d77002fb783

Public Version Date

May 05, 2020

Public Version Number

5

DI Record Publish Date

December 09, 2015

Package DI Number

20026072001305

Quantity per Package

6

Contains DI Package

00026072001301

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case