Catalog Number

MPC-720

Brand Name

Molded Products, Inc.

Version/Model Number

MPC-720

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K010712,K010712,K010712

Product Code

FID

Product Code Name

Tubing, Dialysate

Public Device Record Key

7ca77291-a1fb-4559-bc30-8a02ff4c32c2

Public Version Date

September 12, 2019

Public Version Number

1

DI Record Publish Date

September 04, 2019

Package DI Number

B144MPC7203

Quantity per Package

20

Contains DI Package

B144MPC7201

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case