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

EJT 1978-12-28

GOLD, 24 KARAT CASTING

Applicant Williams Gold Refining Co., Inc.

K-Number K781788

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EIA 1978-12-28

MODULAT DENTAL SYSTEMS

Applicant Vacudent Sales Corp.

K-Number K781882

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ETF 1978-12-28

TABLE, EXAMINING-TWO EIGHTY

Applicant Amsco Co.

K-Number K782064

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HQF 1978-12-28

LASER, PHOTOCOAGULATION

Applicant Cavitron Corp.

K-Number K782065

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DXY 1978-12-27

PACEMAKER, MODEL DDP ELECTRONIC CIRCUIT

Applicant Arco Medical Products Co.

K-Number K782146

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N/A 1978-12-27

SPONGE SYSTEM, ROSERING CONTAIN-COUNT

Applicant Medline Industries, Inc.

K-Number K782120

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BYE 1978-12-26

VALVE, AMBU PEEP

Applicant Narco Air-Shields

K-Number K782152

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KLK 1978-12-26

MONITOR, SENSOMATIII OXYGEN

Applicant Biochem International, Inc.

K-Number K781910

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DTD 1978-12-22

ELECTRODE LEAD MODEL 030-198

Applicant Telectronics, Inc.

K-Number K782097

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DXY 1978-12-22

MICROLITH A MODEL 803

Applicant Cardiac Pacemakers, Inc.

K-Number K782023

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IYX 1978-12-22

MAXI CAMERA 400T

Applicant General Electric Co.

K-Number K782029

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DXY 1978-12-22

MICROLITH A MODEL 703

Applicant Cardiac Pacemakers, Inc.

K-Number K782022

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