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

KLK 1981-06-12

LIFESPAN 100

Applicant Biochem International, Inc.

K-Number K811470

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JSK 1981-06-12

HUMAN BLOOD IN ALSEVER'S

Applicant Dutchland Laboratories, Inc.

K-Number K811225

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KRA 1981-06-12

MEDI-TRACE

Applicant Graphic Controls Corp.

K-Number K811410

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IQI 1981-06-12

FOREARM & KNEE STRAPS

Applicant Fred Sammons, Inc.

K-Number K811490

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KDJ 1981-06-12

GAMBRO PERITONEAL DIALYSIS FLUID LINES

Applicant Gambro, Inc.

K-Number K811294

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FJG 1981-06-12

EXP 200 PARALLEL PLATE DIALYZER

Applicant Extracorporeal Medical Specialities, Inc.

K-Number K811439

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EMA 1981-06-12

HY-BOND POLYCARBOXYLATE CEMENT

Applicant Shofu Dental Corp.

K-Number K810764

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KPR 1981-06-12

KERMATH RADIOGRAPHIC HEAD STAND

Applicant Kermath Mfg. Corp.

K-Number K811215

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DRS 1981-06-12

MODELS TA 1017 & 1017T GRITIFLO DISPOS

Applicant Gould, Inc.

K-Number K811538

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FMF 1981-06-12

PREFILLED PULSATOR SYRINGE

Applicant Concord Laboratories, Inc.

K-Number K811009

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EMA 1981-06-12

HY-BOND ZINC PHOSPHATE CEMENT

Applicant Shofu Dental Corp.

K-Number K810765

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KNX 1981-06-12

MMG URINARY DRAINAGE TUBING

Applicant Medical Marketing Group

K-Number K811469

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