Catalog Number

-

Brand Name

Plastcare

Version/Model Number

CLB

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

DYN

Product Code Name

Mouthpiece, Saliva Ejector

Public Device Record Key

35ae6efe-aff1-45c9-9222-5793dd8577c1

Public Version Date

March 18, 2020

Public Version Number

1

DI Record Publish Date

March 10, 2020

Package DI Number

D915CLB2

Quantity per Package

10

Contains DI Package

D915CLB1

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-