Catalog Number

13-240

Brand Name

CROWN SURGICAL

Version/Model Number

CLAMPS

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GDJ

Product Code Name

Clamp, Surgical, General & Plastic Surgery

Public Device Record Key

2416bab3-752a-4eb9-9809-6179c9e52af5

Public Version Date

March 10, 2021

Public Version Number

1

DI Record Publish Date

March 02, 2021

Package DI Number

B924132402

Quantity per Package

500

Contains DI Package

B924132400

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARDBOARD BOX