Catalog Number

-

Brand Name

NA

Version/Model Number

D-lite Spirometry Kit 2m 7ft, 8004381

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

BZK

Product Code Name

Spirometer, monitoring (w/wo alarm)

Public Device Record Key

9a613d2d-6642-47ca-8a2c-dccfa5760022

Public Version Date

August 05, 2022

Public Version Number

8

DI Record Publish Date

August 15, 2016

Package DI Number

20840682102876

Quantity per Package

20

Contains DI Package

00840682102872

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-