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CorVista® System

FDA UDI

Class II (US FDA UDI)

by Analytics For Life, Inc.

Identity

Trade Name
CorVista® System FDA UDI
Generic Name
Multiparameter physiologic analysis workstation FDA UDI
Device Name
CorVista® System with CAD Add-On FDA UDI
Model / Reference
10-0020 FDA UDI
Description
CorVista® System with CAD Add-On FDA UDI

Identifiers

Primary DI / UDI-DI
00869059000429 FDA UDI
510(k) Number
K232686 FDA UDI
FDA Product Code
QXX FDA UDI
DQK FDA UDI
GMDN Term
Multiparameter physiologic analysis workstation FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2380 FDA UDI
870.1425 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multiparameter physiologic analysis workstation

CorVista® System by Analytics For Life, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiparameter physiologic analysis workstation.

Cleared under the same submission

K232686 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Analytics For Life, Inc.

Sources (1)

  • FDA UDI 4dd4b724-b8aa-4999-acfa-7fed0410730b 36 fields · synced Jun 8, 2026