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510(k) Data Aggregation

K Number

Device Name

P.H.D. - PERSONAL HEART DEVICE MODEL 5258

Manufacturer

HEART ALERT, INC.

Date Cleared

1997-05-15

(227 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

Why did this record match?

Applicant Name (Manufacturer) :

HEART ALERT, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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