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510(k) Data Aggregation

K Number

Device Name

TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001

Manufacturer

Date Cleared

2000-05-08

(90 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

Why did this record match?

Device Name :

TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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