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Found 2 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

REUSABLE GLASS SYRINGES

Manufacturer

LOCKETT MEDICAL CORP.

Date Cleared

2001-08-10

(115 days)

Product Code

Regulation Number

Type

Panel

General Hospital

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

STERILE WATER O.9% STERILE SALINE

Manufacturer

LOCKETT MEDICAL CORP.

Date Cleared

1996-01-24

(100 days)

Product Code

Regulation Number

Type

Panel

General Hospital

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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