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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

FIRARD II/ TDP LAMP

Manufacturer

HELIO MEDICAL SUPPLIES, INC.

Date Cleared

1996-06-06

(156 days)

Product Code

Regulation Number

Type

Panel

Physical Medicine

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K020851,K053376,K060076,K081720

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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