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

EJS 1981-08-18

BAK-ON SP PORCELAIN ALLOY

Applicant Johnson & Johnson Professionals, Inc.

K-Number K812101

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IYO 1981-08-18

NEEDLE GUIDE ATTACHMENT

Applicant Technicare Corp.

K-Number K811931

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HNW 1981-08-18

KOI LACREMAL HOOK & DILATOR

Applicant Koi, Inc.

K-Number K812097

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GKJ 1981-08-18

HEMASPINNER

Applicant Geometric Data, Div. Smithkline Corp.

K-Number K811534

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JPD 1981-08-18

HELENA SICKLE-THAL QUIK COLUMN METHOD

Applicant Helena Laboratories

K-Number K812077

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BYI 1981-08-18

PERCUSSOR

Applicant Dhd Medical Products Div. Diemolding Corp.

K-Number K812166

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FTC 1981-08-17

UVA SUN TANNING EQUIPMENT

Applicant Cpc Systems, Inc.

K-Number K811870

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ITM 1981-08-13

POLI-AXIAL KNEE CAGE

Applicant Generation II Orthotics, Inc.

K-Number K812064

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JTO 1981-08-13

KANAMYCIN DISK

Applicant Remel Co.

K-Number K812082

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GTQ 1981-08-13

BI-ASO SLIDE TEST

Applicant Biologics Intl., Inc.

K-Number K812060

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DTB 1981-08-13

PACEPATH IMPLANTABLE ENDOCARD. PACING LD

Applicant Pacesetter Systems

K-Number K811200

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CGA 1981-08-13

GLUCOSE OXIDASE RATE REAGENT

Applicant Chem-Elec, Inc.

K-Number K811165

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