Catalog Number

-

Brand Name

Plastcare

Version/Model Number

RIT-5030

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KYX

Product Code Name

Dispenser, Liquid Medication

Public Device Record Key

7b659e22-3a63-483f-b048-0c12d0b85ca0

Public Version Date

March 04, 2020

Public Version Number

1

DI Record Publish Date

February 25, 2020

Package DI Number

D915RIT50302

Quantity per Package

20

Contains DI Package

D915RIT50301

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-