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

EFQ 1979-03-26

SURGICAL EYE SPONGE

Applicant Medtech Intl., Inc.

K-Number K790467

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JDL 1979-03-26

BG PROXIMAL FEMUR

Applicant Howmedica Corp.

K-Number K790274

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GDY 1979-03-26

GAUZE & COTTON SPONGES

Applicant Medtech Intl., Inc.

K-Number K790389

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IZL 1979-03-26

510 CARBINETTE X-RAY UNIT

Applicant General X-Ray, Inc.

K-Number K790392

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IYE 1979-03-26

MEVATRON 60

Applicant Siemens Medical Laboratories, Inc.

K-Number K790388

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IYX 1979-03-26

MODU-SET COLLIMOTOR

Applicant Medtronic Vascular

K-Number K790463

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IZL 1979-03-26

PORTABLE X-RAY UNIT

Applicant General X-Ray, Inc.

K-Number K790512

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BSZ 1979-03-23

SERIES 7000

Applicant Narco Mckesson Co.

K-Number K790456

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DRL 1979-03-23

DEFIBRILLATOR INTERAL PADDLE TEST LOAD

Applicant Physio-Control Corp.

K-Number K790394

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CBC 1979-03-23

AMBU SUCTION BOOSTER

Applicant Narco Air-Shields

K-Number K790035

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DSH 1979-03-23

CARDIOCASSETTE II, AMBULATORY ECG SYSTEM

Applicant Cambridge Instruments, Inc.

K-Number K790509

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KRA 1979-03-23

MICROFLUSH

Applicant Medex, Inc.

K-Number K790455

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