HEMOSURE® - Hemosure FOB Test 50 Cassettes and 50 Collection - HEMOSURE INC.

Duns Number:806777541

Device Description: Hemosure FOB Test 50 Cassettes and 50 Collection Tubes per Box Kit without Mailer (Made in Hemosure FOB Test 50 Cassettes and 50 Collection Tubes per Box Kit without Mailer (Made in USA)

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More Product Details

Catalog Number

T1-CK50US

Brand Name

HEMOSURE®

Version/Model Number

T1-CK50US

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

KHE

Product Code Name

Reagent, Occult Blood

Device Record Status

Public Device Record Key

e31e8edc-6916-457f-a000-f9146538f130

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

March 23, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HEMOSURE INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 4
2 A medical device with a moderate to high risk that requires special controls. 7