Catalog Number

M52321

Brand Name

Ponto

Version/Model Number

M52321

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 15, 2017

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LXB

Product Code Name

Hearing Aid, Bone Conduction

Public Device Record Key

5ec51ba9-7d35-46e4-9d3b-a50e7b533bfc

Public Version Date

October 16, 2020

Public Version Number

3

DI Record Publish Date

September 16, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-