Clear Guide CORE - The device is intended as a computer platform to - CLEAR GUIDE MEDICAL, INC.

Duns Number:965399905

Device Description: The device is intended as a computer platform to perform computation, display, connectivit The device is intended as a computer platform to perform computation, display, connectivity and user input functions for CLEAR GUIDE image guidance software (e.g., Clear Guide SCENERGY). The device facilitates rigid, needle-like surgical instrument tracking and guidance feedback for diagnostic and interventional procedures in a clinical setting. The CG-CORE24 model is a panel PC with a 24" screen.

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More Product Details

Catalog Number

CG-CORE24

Brand Name

Clear Guide CORE

Version/Model Number

CGCORE24

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K153004,K153004

Product Code Details

Product Code

JAK

Product Code Name

System, X-Ray, Tomography, Computed

Device Record Status

Public Device Record Key

a0698437-57ee-47ad-84e8-4dba67b2db7d

Public Version Date

October 17, 2022

Public Version Number

1

DI Record Publish Date

October 07, 2022

Additional Identifiers

Package DI Number

B201CGCORE241

Quantity per Package

1

Contains DI Package

B201CGCORE240

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"CLEAR GUIDE MEDICAL, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 4