Catalog Number

PG-MA-1000

Brand Name

PlastCare

Version/Model Number

PG-MA-1000

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

KXR

Product Code Name

Applicator, Resin

Public Device Record Key

a638c8ad-8fb8-4b63-95a2-db2b7d063eed

Public Version Date

July 12, 2021

Public Version Number

1

DI Record Publish Date

July 02, 2021

Package DI Number

D066PGMA10002

Quantity per Package

40

Contains DI Package

D066PGMA10001

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-