Catalog Number

-

Brand Name

DC300 Diagnostic chamber

Version/Model Number

VD0702104

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

-

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

8cc5c784-49e2-4a53-a713-cf477a5fb40b

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 21, 2016

Package DI Number

EIBAVD07021041

Quantity per Package

1

Contains DI Package

EIBAVD07021040

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

chamber case