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

KMI 1977-07-14

MONITOR, BED, TECHNOLICS

Applicant Technolics, Inc.

K-Number K770695

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FRC 1977-07-14

KENWOOD BIOLOGICAL STEOILIZ. INDICATOR

Applicant Will Ross Co.

K-Number K771132

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JKH 1977-07-14

COLORIMETRIC DETERM. SOCITRATE DEHYDRO.

Applicant Sigma Chemical Co.

K-Number K770902

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FMF 1977-07-14

SYRINGE, BLOOD SAMPLING, ARTERIAL, #4016

Applicant Concord Laboratories, Inc.

K-Number K770851

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ETS 1977-07-14

REVERSING CLICK GENERATOR RCG6

Applicant Teca, Inc.

K-Number K771188

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FMI 1977-07-14

DISP. HYPODERMIC NEEDLE

Applicant Terumo America, Inc.

K-Number K771203

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CDT 1977-07-14

TRIGLYCERIDE ENZYMATIC METHOD

Applicant Union Carbide Corp.

K-Number K770841

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N/A 1977-07-14

ULTRAZYME PLUS GOT

Applicant Harleco

K-Number K770883

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KKX 1977-07-14

SURGICAL HEAD DRAPE, DISP.

Applicant Procter & Gamble Mfg. Co.

K-Number K771136

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HDG 1977-07-14

VAGINAL ILLUMINATOR, MODEL 78570

Applicant Welch Allyn, Inc.

K-Number K771181

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CKA 1977-07-14

ULTRAZYME PLUS GPT

Applicant Harleco

K-Number K770882

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CDX 1977-07-14

QUANTIMUNE NEONATAL & THYROXINE RIA

Applicant Bio-Rad

K-Number K771135

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