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

KOC 1983-06-30

HAEMOLYTE SOLUTION

Applicant Dialysis Clinic, Inc.

K-Number K831409

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DWF 1983-06-30

AORTIC ROOT CANNULA W/INTEGRAL PRESS

Applicant Dlp, Inc.

K-Number K831591

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ILI 1983-06-30

ARM SLINGS

Applicant Fred Sammons, Inc.

K-Number K831549

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LIF 1983-06-30

SPORIDIDIN-D COLD STERILIZING/SOLUTION

Applicant Sporicidin Intl.

K-Number K830722

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HPN 1983-06-30

RARE-EARTH INTRA-OCULAR MAGNET

Applicant Miami Eye Technology, Inc.

K-Number K831702

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HHF 1983-06-30

RELIANCE TEMPO OPHTH. INSTR STAND

Applicant F. & F. Koenigkramer

K-Number K831568

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ESD 1983-06-30

CUSTOM IN-THE-EAR HEARING AID

Applicant Finetone Hearing Instruments

K-Number K830960

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JTO 1983-06-30

OXY-SWAB

Applicant Austin Biological Laboratories

K-Number K831673

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DQO 1983-06-30

SONTEK INFUSION CATHETER

Applicant Sontek Corp.

K-Number K831562

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LXP 1983-06-30

SCLERAL PLUG

Applicant Medical Instrument Development Laboratories, Inc.

K-Number K831193

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FRN 1983-06-30

FLO-GARD 6100 VOLUMETRIC INFUSION PUMP

Applicant Travenol Laboratories, S.A.

K-Number K831258

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DWF 1983-06-30

ARGYLE DUAL STAGE VENOUS RETURN CATH.

Applicant Sherwood Medical Co.

K-Number K831332

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