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

IYY 1979-03-22

GENERATOR, R-WAVE

Applicant Amr Co.

K-Number K790213

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JAK 1979-03-22

SOMATOM SD

Applicant Siemens Corp.

K-Number K790342

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JAY 1979-03-22

ADULT ZEE-FRAME

Applicant Equilibrated Bio Systems, Inc.

K-Number K790410

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CBN 1979-03-22

NAD SCAVENGING RELIEF VALVE

Applicant Draeger Medical, Inc.

K-Number K790333

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JFA 1979-03-22

BURNETT-KETCHUM DYNAMIC HAND EXERCISER

Applicant Maddak, Inc.

K-Number K790527

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HEB 1979-03-22

KOTEX TUBE AND STICK TAMPON

Applicant Kimberly-Clark Corp.

K-Number K790385

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KWQ 1979-03-21

SPINAL SURGERY INSTRUMENTATION

Applicant Stuart Drug & Surgical Supply, Inc.

K-Number K782061

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KWQ 1979-03-21

DTT SYSTEM

Applicant Depuy, Inc.

K-Number K790404

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FIE 1979-03-21

A.V. FISTULA NEEDLE SET

Applicant Cordis Corp.

K-Number K782021

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JPA 1979-03-21

COAG-A-MATE 2001

Applicant General Diagnostics

K-Number K790323

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KKX 1979-03-21

DRAPES, DISPOSABLE SURGICAL

Applicant Marco Mfg.

K-Number K782051

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GGM 1979-03-21

HEMOGLOBIN CONTROLS

Applicant Electrophoresis Corp.

K-Number K790310

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