Catalog Number

-

Brand Name

Whicam M

Version/Model Number

IC-WHMA90

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

KQM

Product Code Name

Camera, Surgical And Accessories

Public Device Record Key

b4a60d4a-c308-4ee4-a453-f206c168f244

Public Version Date

November 07, 2019

Public Version Number

1

DI Record Publish Date

October 30, 2019

Package DI Number

18800025400149

Quantity per Package

1

Contains DI Package

08800025400142

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-