Catalog Number

-

Brand Name

NA

Version/Model Number

S2509-7100

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 03, 2018

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

-

Product Code

FNM

Product Code Name

Mattress, Air Flotation, Alternating Pressure

Public Device Record Key

e1d6305a-6dc5-4550-bd92-85940cbb17b3

Public Version Date

October 03, 2018

Public Version Number

3

DI Record Publish Date

March 22, 2017

Package DI Number

04713616091275

Quantity per Package

10

Contains DI Package

04713616093743

Package Discontinue Date

October 03, 2018

Package Status

Not in Commercial Distribution

Package Type

-