Catalog Number

13000502

Brand Name

Spacelabs Healthcare

Version/Model Number

VAPORIZER

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K942799

Product Code

CAD

Product Code Name

VAPORIZER, ANESTHESIA, NON-HEATED

Public Device Record Key

dedd1f5b-8155-4476-833a-23539e56b3b6

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-