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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

HARVEST TECHNOLOGIES DUAL LIQUID APPLICATOR, MODEL SK/S: HARVEST DUAL LIQUID APPLICATOR LK/2

Manufacturer

HARVEST TECHNOLOGIES, LLC.

Date Cleared

2000-06-01

(111 days)

Product Code

Regulation Number

Type

Panel

General Hospital

Age Range

N/A

Reference & Predicate Devices

N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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