Venti-Scan IV Convenience Kit, Venti Pak - Venti-Scan IV Convenience Kit, Venti Pak, part of - CAPINTEC, INC.

Duns Number:047684501

Device Description: Venti-Scan IV Convenience Kit, Venti Pak, part of Radioaerosol Administration System

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More Product Details

Catalog Number

177-075

Brand Name

Venti-Scan IV Convenience Kit, Venti Pak

Version/Model Number

177-075

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

K871868

Product Code Details

Product Code

IYT

Product Code Name

System, Rebreathing, Radionuclide

Device Record Status

Public Device Record Key

fafb5078-5fa1-4b61-a26a-22965ad23ee1

Public Version Date

August 16, 2022

Public Version Number

1

DI Record Publish Date

August 08, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CAPINTEC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 81
2 A medical device with a moderate to high risk that requires special controls. 17