Catalog Number

-

Brand Name

Precept®

Version/Model Number

15100

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LYU

Product Code Name

Accessory, Surgical Apparel

Public Device Record Key

99ee7fcf-d5d8-40cc-9406-edfcb20b97c7

Public Version Date

May 06, 2020

Public Version Number

2

DI Record Publish Date

September 18, 2018

Package DI Number

20814707020605

Quantity per Package

10

Contains DI Package

10814707020608

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-