Catalog Number

na

Brand Name

LC Plus

Version/Model Number

022F81-PRO

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K935540,K935540

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

7dbd805a-522c-455e-8253-45cf0a2112f9

Public Version Date

April 15, 2020

Public Version Number

1

DI Record Publish Date

April 07, 2020

Package DI Number

00744229100720

Quantity per Package

50

Contains DI Package

00744229229575

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton