Catalog Number

SARP-36

Brand Name

SJM™

Version/Model Number

SARP-36

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K092310

Product Code

KRH

Product Code Name

RING, ANNULOPLASTY

Public Device Record Key

48eacbed-ad32-4036-899f-c1e17664b977

Public Version Date

February 05, 2021

Public Version Number

5

DI Record Publish Date

December 04, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-