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

FLI 1979-05-07

EO EVACUATING SYSTEM I

Applicant Castle Co.

K-Number K790677

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IYE 1979-05-04

MEVATRON 74

Applicant Siemens Medical Laboratories, Inc.

K-Number K790747

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KKX 1979-05-04

TREATED BARRIER INCISE DRAPE

Applicant Surgikos, Inc.

K-Number K790431

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FPA 1979-05-04

CUSTOM TUBING SETS

Applicant Norton Performance Plastics Corp.

K-Number K790604

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IZL 1979-05-04

OMNIMEDICAL AUTOMATIC 1001

Applicant Omnimedical

K-Number K790673

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CBP 1979-05-04

NON-REBREATHING T PIECE

Applicant Dhd Medical Products Div. Diemolding Corp.

K-Number K790820

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KSZ 1979-05-04

ELDONCARD

Applicant Nordisk Infuser System

K-Number K790282

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CBK 1979-05-04

VS, ANESTHESIA VENTILATOR

Applicant Airco/Ohio Medical Products

K-Number K790809

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JLS 1979-05-03

PROGESTERONE

Applicant Serono Laboratories, Inc.

K-Number K790440

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JXR 1979-05-03

ATOMIC ABSORPTION SPECTROPHOTOMETER,

Applicant Varian Assoc., Inc.

K-Number K790780

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JTB 1979-05-03

I NETILMICIN RIA KIT

Applicant Diagnostic Products Corp.

K-Number K790514

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CDX 1979-05-03

THYROXINE RIA KIT

Applicant Technia Diagnostics , Ltd.

K-Number K790495

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