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Found 2 results

510(k) Data Aggregation

K Number

Device Name

MODEL 5000 MULTIPLACE HYPERBARIC THERAPY

Manufacturer

HYPERTEC, INC.

Date Cleared

2000-12-06

(90 days)

Product Code

CBF

Regulation Number

868.5470

Why did this record match?

Applicant Name (Manufacturer) :

HYPERTEC, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

Ask a Question

K Number

Device Name

MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS

Manufacturer

HYPERTEC, INC.

Date Cleared

2000-12-06

(90 days)

Product Code

CBF

Regulation Number

868.5470

Why did this record match?

Applicant Name (Manufacturer) :

HYPERTEC, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

Ask a Question

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