Vasomedical-Biox™ CB Series Analysis & Reporting Software - 3 CH ECG & ABP - CB Series Analysis & Reporting S/W - 3 CH ECG & - VASOMEDICAL, INC.

Duns Number:197210248

Device Description: CB Series Analysis & Reporting S/W - 3 CH ECG & Combined ABPM

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More Product Details

Catalog Number

A10-0035

Brand Name

Vasomedical-Biox™ CB Series Analysis & Reporting Software - 3 CH ECG & ABP

Version/Model Number

CB Series S/W

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

K111180

Product Code Details

Product Code

DSH

Product Code Name

RECORDER, MAGNETIC TAPE, MEDICAL

Device Record Status

Public Device Record Key

01bc62ec-fd0a-4f7f-b4d6-9f80172d400b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 29, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"VASOMEDICAL, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 146