Leica Biosystems CytoVision V7.5 configuration - Leica Biosystems CytoVision V7.5 configuration - Leica Biosystems Richmond, Inc.

Duns Number:082930884

Device Description: Leica Biosystems CytoVision V7.5 configuration

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More Product Details

Catalog Number

-

Brand Name

Leica Biosystems CytoVision V7.5 configuration

Version/Model Number

23SWR00075CV

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

-

Product Code Details

Product Code

JOY

Product Code Name

DEVICE, AUTOMATED CELL-LOCATING

Device Record Status

Public Device Record Key

d57250a6-0eab-4c7b-8f76-f58882acbfa7

Public Version Date

March 22, 2022

Public Version Number

3

DI Record Publish Date

April 27, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"LEICA BIOSYSTEMS RICHMOND, 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. 206