Catalog Number

OS-LPCD

Brand Name

Lap-port closure device

Version/Model Number

OS-LPCD

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GCJ

Product Code Name

Laparoscope, General & Plastic Surgery

Public Device Record Key

926e2708-0489-4b03-a34a-510f7de88e3a

Public Version Date

August 17, 2021

Public Version Number

4

DI Record Publish Date

November 15, 2016

Package DI Number

B354OSLPCD10

Quantity per Package

10

Contains DI Package

B354OSLPCD0

Package Discontinue Date

November 15, 2019

Package Status

Not in Commercial Distribution

Package Type

-