Catalog Number

1200-392

Brand Name

KAHN-FOMON SCISSORS

Version/Model Number

1200-392

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KBD

Product Code Name

SCISSORS, NASAL

Public Device Record Key

078ca8a4-3ac6-4659-ae1e-3574f502c876

Public Version Date

October 29, 2018

Public Version Number

1

DI Record Publish Date

September 27, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-