Catalog Number

-

Brand Name

Com-Fit®

Version/Model Number

20352

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

Yes

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

-

Product Code

FXX

Product Code Name

Mask, surgical

Public Device Record Key

aa20737e-9e39-4241-bcac-b463e9e1405e

Public Version Date

May 06, 2020

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

D687203522

Quantity per Package

10

Contains DI Package

D687203521

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case