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

KNT 1981-03-31

OESOPHAGEAL THERAPY KIT

Applicant Keymed, Inc.

K-Number K810392

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KOD 1981-03-31

SILICONE ELASTOMER COATED LATEX FOLEY

Applicant G.D. Searle and Co.

K-Number K810630

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KZM 1981-03-31

MODEL EM-IR

Applicant Myo-Tronics Research, Inc.

K-Number K810528

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FDF 1981-03-31

PENTAX COLONOSCOPE MODEL FC-34 MA

Applicant Pentax Precision Instrument Corp.

K-Number K810791

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LFJ 1981-03-31

DOUBLE LUMEN SUBCLAVIN CATHETER SC-400

Applicant Vas-Cath of Canada , Ltd.

K-Number K810745

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JTN 1981-03-31

CEFOTAXIME 30 MCG. SENSI-DISC.

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K810564

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LDQ 1981-03-30

DRESSING CHANGE TRAY-MEDIUM

Applicant Associated Medical Products Co.

K-Number K810570

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IPF 1981-03-30

LITRONIC STIMULATOR

Applicant Med-Western Electronics, Inc.

K-Number K810225

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DQK 1981-03-27

MODEL IM1000 INTEGRATED MONITOR

Applicant Gould, Inc.

K-Number K810731

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FDF 1981-03-27

STOPPERLESS HOT/COLD RUBBER WATER BOTTLE

Applicant First Industries, Inc.

K-Number K810654

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KYR 1981-03-27

VINYL ICE BAG

Applicant First Industries, Inc.

K-Number K810653

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DHI 1981-03-27

HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-

Applicant Serono Laboratories, Inc.

K-Number K810625

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