Catalog Number

706920NS

Brand Name

Spectrum, Inc.

Version/Model Number

982-03561-000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K934630,K934630

Product Code

MMP

Product Code Name

Cover, barrier, protective

Public Device Record Key

f541d7b6-ccf3-42ca-8135-7ec5d31b7e5e

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 30, 2017

Package DI Number

10850301007652

Quantity per Package

100

Contains DI Package

00850301007655

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

shipper