GC CAVITY CONDITIONER - GC CAVITY CONDITIONER 5.7 mL Liquid - Gc America Inc.

Duns Number:005473608

Device Description: GC CAVITY CONDITIONER 5.7 mL Liquid

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More Product Details

Catalog Number

000110

Brand Name

GC CAVITY CONDITIONER

Version/Model Number

000110

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

-

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

K953166,K953166

Product Code Details

Product Code

KLE

Product Code Name

AGENT, TOOTH BONDING, RESIN

Device Record Status

Public Device Record Key

707bad62-0fd8-4e57-aa90-287a2d85965b

Public Version Date

August 29, 2022

Public Version Number

1

DI Record Publish Date

August 19, 2022

Additional Identifiers

Package DI Number

24548161282496

Quantity per Package

10

Contains DI Package

14548161282499

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"GC AMERICA INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 480
2 A medical device with a moderate to high risk that requires special controls. 4772