Catalog Number

5839

Brand Name

3M™ Littmann® Classic III™

Version/Model Number

5839

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LDE

Product Code Name

STETHOSCOPE, MANUAL

Public Device Record Key

4560688f-5936-4217-9881-0e38b04c6240

Public Version Date

August 24, 2021

Public Version Number

1

DI Record Publish Date

August 16, 2021

Package DI Number

50707387789713

Quantity per Package

3

Contains DI Package

00707387789718

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX