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

DRT 1979-04-03

MODEL 78801A PATIENT MONITORS

Applicant Hewlett-Packard Co.

K-Number K790454

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GCP 1979-04-02

ENDOSCOPE AND ACCESSORIES

Applicant Olympus Corp.

K-Number K790071

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DTB 1979-03-29

MEDTRONIC MODEL 6971

Applicant Medtronic Vascular

K-Number K790074

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JAK 1979-03-28

VIDICAM VIDEO REPROGRAPH

Applicant Vidicam

K-Number K790395

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KXJ 1979-03-28

CLEARVIEW

Applicant Hipoint Research, Inc.

K-Number K790536

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N/A 1979-03-28

IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI

Applicant Shiley, Inc.

K-Number K790425

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IZL 1979-03-28

X-RAY UNITS, GX-101, UCIS-510 AND GX-111

Applicant General X-Ray, Inc.

K-Number K790451

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JDI 1979-03-28

INTERPLANTA SP TOTAL HIP PROSTHESIS

Applicant Waldemar Link GmbH & Co. KG

K-Number K790488

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IYX 1979-03-28

U-MAT

Applicant Engineering Dynamics Corp.

K-Number K790466

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JSG 1979-03-28

CEMENT DISPENSER CEMENT MIXER

Applicant Dow Corning Wright

K-Number K790459

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CAP 1979-03-28

BUNN MODEL #40 LOW PRESSURE ALARM

Applicant The John Bunn Co.

K-Number K790370

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KRJ 1979-03-28

RECIRCULATION FILTER MODEL RF-10

Applicant Bentley Laboratories, Inc.

K-Number K790361

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