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

CFM 1982-03-25

CORNING 902 SODIUM POTASSIUM ANALYZER

Applicant Corning Medical & Scientific

K-Number K820629

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FMI 1982-03-25

HYPODERMIC & SUTURE NEEDLES

Applicant Needle Industries(Usa), Inc.

K-Number K813256

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FAP 1982-03-23

DISA WATER CYSTOMETER

Applicant Disa Electronics

K-Number K820144

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KOD 1982-03-23

AM. PH. STERILE SINGLE-USE URETHRAL CATH

Applicant American Pharmaseal Div. Ahsc

K-Number K820419

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FIF 1982-03-23

COBE SINGLE-NEEDLE CONTROLLER #18-756

Applicant Cobe Laboratories, Inc.

K-Number K820173

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LIF 1982-03-23

COMPUDIAL/KP-1

Applicant Computer Dialysis Systems, Inc.

K-Number K813107

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EJK 1982-03-23

IMPROVED DYCAL

Applicant Dentsply Intl.

K-Number K820215

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GWQ 1982-03-23

OTE BIOMEDICA NEUROGRAPH 9

Applicant Del Mar Avionics

K-Number K820604

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DWO 1982-03-23

RNG SERIES ULTRASOUND NEEDLE/CATH. GDS

Applicant CIVCO Medical Instruments Co., Inc.

K-Number K820269

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FKT 1982-03-23

SORB II

Applicant Organon Teknika Corp.

K-Number K813574

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BWN 1982-03-23

ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL

Applicant David Simmonds Co., Inc.

K-Number K820574

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BZL 1982-03-23

MGC/LITTON 2300

Applicant Medical Graphics Corp.

K-Number K820475

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