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510(k) Data Aggregation

K Number

Device Name

OSCAR 2, MODEL 222

Manufacturer

SUNTECH MEDICAL INSTRUMENTS, INC.

Date Cleared

2000-10-25

(30 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

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Device Name :

OSCAR 2, MODEL 222

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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