Catalog Number

36-MPE8200EU

Brand Name

MicroMedical

Version/Model Number

36-MPE8200EU

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 23, 2019

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

K030586

Product Code

BZH

Product Code Name

Meter, Peak Flow, Spirometry

Public Device Record Key

c2d6cab1-c12c-4f49-8b9f-bfd67d0dd127

Public Version Date

March 16, 2021

Public Version Number

5

DI Record Publish Date

March 31, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-