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Found 2 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS

Manufacturer

Date Cleared

2000-12-06

(90 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K021693,K081506

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

MODEL 5000 MULTIPLACE HYPERBARIC THERAPY

Manufacturer

Date Cleared

2000-12-06

(90 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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