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

JOW 1978-09-20

T.E.D. SEQUENTIAL COMPRESSION SLEEVES

Applicant Kendall Research Center

K-Number K781357

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KXA 1978-09-20

TILLMAN HIPSURFACE REPLACEMENT

Applicant Waldemar Link GmbH & Co. KG

K-Number K781490

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JOW 1978-09-20

SEQUENTIAL CUFF INFLATION DEVICE

Applicant Medasonics, Inc.

K-Number K781358

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GBO 1978-09-20

SILASTIC U-TUBE KIT

Applicant Dow Corning Corp. Healthcare Industries Materials

K-Number K781526

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HNN 1978-09-20

MICROSURGICAL KNIVES, 20, 30, 45

Applicant Codman & Shurtleff, Inc.

K-Number K781465

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HRH 1978-09-20

CORNEAL CUTTER AND ACCESSORIES

Applicant Codman & Shurtleff, Inc.

K-Number K781411

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DZS 1978-09-20

MERCURY DISP. CAPSULE

Applicant Lee Pharmaceuticals

K-Number K781243

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JXA 1978-09-20

MS-2 AUTOMATED URINE SCREENING SYSTEM

Applicant Abbott Laboratories

K-Number K781370

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KOD 1978-09-20

FOLEY CATHETERS

Applicant Intermed, Inc.

K-Number K781457

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GAA 1978-09-20

BONE MARROW ASPIRATION KIT

Applicant Ferris Mfg. Corp.

K-Number K781371

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DRT 1978-09-20

DIGITAL PANEL METER

Applicant Rae Medical Corp.

K-Number K781255

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JJS 1978-09-20

BIOSCAN E12

Applicant Clinifax Industries, Ltd.

K-Number K781421

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