Catalog Number

08010-00

Brand Name

Innomed, Inc.

Version/Model Number

8010-00

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

-

Product Code

FCW

Product Code Name

Light Source, Fiberoptic, Routine

Public Device Record Key

87c83a3b-ef6c-4c6b-aa61-b82532683f0a

Public Version Date

February 09, 2021

Public Version Number

2

DI Record Publish Date

June 30, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-