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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

ALTERNATING PRESSURE AIR FLOTATION MATTRESS

Manufacturer

DECUBITI CONCEPTS, INC.

Date Cleared

1997-07-31

(52 days)

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Regulation Number

Type

Panel

General Hospital

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N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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