Catalog Number

P807179

Brand Name

Baha

Version/Model Number

P807179

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 01, 2020

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

-

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

K171088

Product Code

LXB

Product Code Name

Hearing aid, bone conduction

Public Device Record Key

c3339df9-0cdf-4a6f-adde-c1fa34593443

Public Version Date

April 06, 2020

Public Version Number

5

DI Record Publish Date

November 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-