Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

CIX 1983-06-16

ALBUMIN REAGENT (BCG

Applicant Reagents Applications, Inc.

K-Number K831585

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HHD 1983-06-16

MODIFIED UNSCENTED MENSTRUAL PADS

Applicant Personal Products Co.

K-Number K831707

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DXQ 1983-06-16

VASCULAB BLOOD PRESSURE CUFF

Applicant Medasonics, Inc.

K-Number K831393

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CHL 1983-06-16

ELECTROLYLE CARBON DIOXIDE ELECTRODES

Applicant Fisher Scientific Co., LLC

K-Number K831025

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LFL 1983-06-16

NEEDLE GUIDE MODEL 21285A

Applicant Hewlett-Packard Co.

K-Number K830753

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GCJ 1983-06-16

UNIVERSAL CANNULA

Applicant Acufex Microsurgical, Inc.

K-Number K830719

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CHL 1983-06-16

CALIBRATING SOLUTION FOR ABL-1 & 2

Applicant Fisher Scientific Co., LLC

K-Number K831021

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CHL 1983-06-16

PH 6.838 REF. BUFFER

Applicant Fisher Scientific Co., LLC

K-Number K831019

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FRF 1983-06-16

BREATHING ZONE

Applicant Upper Four, Inc.

K-Number K831067

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EJT 1983-06-16

DOMINION

Applicant Unitek Corp.

K-Number K831098

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GKJ 1983-06-16

E-Z PREP

Applicant Coulter Electronics, Inc.

K-Number K831558

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HHL 1983-06-16

MAXI PADS SCENTED DEODORIZED

Applicant Int'L Consumer Disposables

K-Number K831693

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