UScreen® - U-Screen Squared Integrated Cup with Adulterants - Instant Technologies, Inc.

Duns Number:019410187

Device Description: U-Screen Squared Integrated Cup with Adulterants (CR/Ni/pH) 10 Panel Drug Screen (AMP1000/ U-Screen Squared Integrated Cup with Adulterants (CR/Ni/pH) 10 Panel Drug Screen (AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MTD300/OPI2000/OXY100/PCP25)

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More Product Details

Catalog Number

USSCupA-10NT

Brand Name

UScreen®

Version/Model Number

USSCupA-10NT

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K182701,K182701

Product Code Details

Product Code

LCM

Product Code Name

Enzyme Immunoassay, Phencyclidine

Device Record Status

Public Device Record Key

b5c3d90d-b26c-431b-8ed2-7554d153717e

Public Version Date

October 31, 2022

Public Version Number

5

DI Record Publish Date

May 19, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INSTANT TECHNOLOGIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 122
U Unclassified 1