Catalog Number

3200T

Brand Name

Littmann®

Version/Model Number

3200T

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K083903,K083903

Product Code

DQD

Product Code Name

STETHOSCOPE, ELECTRONIC

Public Device Record Key

c6980307-f3b0-4eb1-ba4f-93a523a8af4d

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

50707387770414

Quantity per Package

3

Contains DI Package

00707387770419

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX