Catalog Number

HS NOTA16200-IN

Brand Name

HS NOTA

Version/Model Number

HS NOTA

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K131925,K131925

Product Code

FCG

Product Code Name

Biopsy Needle

Public Device Record Key

42d48672-440f-4b6f-843f-af439e8eb7f5

Public Version Date

March 09, 2021

Public Version Number

1

DI Record Publish Date

March 01, 2021

Package DI Number

38058983744063

Quantity per Package

10

Contains DI Package

08058983744062

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-