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510(k) Data Aggregation

K Number

Device Name

Manufacturer

LIFE-TECH, INC.

Date Cleared

2010-03-16

(127 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

Why did this record match?

Device Name :

VESISCAN

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

The Vesiscan is used to measure bladder volume.

Device Description

Not Found

AI/ML Overview

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