Catalog Number

-

Brand Name

MediSourceNet, Inc

Version/Model Number

P9552F-MSN

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

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

K073360,K073360,K073360

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

3dfafc8d-0e7b-46e1-8d2e-c1df6e9069aa

Public Version Date

September 14, 2022

Public Version Number

1

DI Record Publish Date

September 06, 2022

Package DI Number

10850034735143

Quantity per Package

25

Contains DI Package

00850034735146

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Box