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

FMZ 1982-01-22

NEOCARE BABY-CONTROLLED INCUBATOR

Applicant Vickers America Medical Corp.

K-Number K813238

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N/A 1982-01-22

TOTAL HEMOLYTIC COMPLEMENT TEST KIT

Applicant Meloy Laboratories, Inc.

K-Number K820005

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CAI 1982-01-22

DISPOSABLE ADULT ANES. CIRCUIT

Applicant Intec.

K-Number K813382

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CFT 1982-01-22

LEECO PRL-QUANT DIAGNOSTIC TEST KIT

Applicant Leeco Diagnostics, Inc.

K-Number K820039

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FLL 1982-01-22

SERIES 400 DISPOSABLE TEMPERATURE PROBE

Applicant Yellow Springs Instrument Co., Inc.

K-Number K813639

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GDY 1982-01-22

PRE-PACK TENS

Applicant Cunningham Woodland, Inc.

K-Number K813286

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EQN 1982-01-22

CONPHAR LARYNGOSCOPE

Applicant Conphar, Inc.

K-Number K813297

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DQO 1982-01-22

SIMPSON-ROBERT CORONARY GUIDING CATHET

Applicant Advanced Catheter Systems

K-Number K813623

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N/A 1982-01-22

REGU-VAC OXYGENATING SUCTION CATHETER

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K813220

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BZK 1982-01-22

SPIROX H

Applicant Cairco , Ltd.

K-Number K812956

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DJD 1982-01-22

TDX PRIMIDONE

Applicant Abbott Laboratories

K-Number K813597

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DQY 1982-01-22

ARROW JUGULAR PUNCTURE KIT 16 GA.

Applicant Arrow Intl., Inc.

K-Number K820009

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