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

DXY 1977-09-12

PACEMAKER MODEL 251

Applicant Intermedics, Inc.

K-Number K771626

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EXR 1977-09-07

DOVER URINE METER

Applicant Will Ross Co.

K-Number K771561

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KCX 1977-09-06

ELECTRONIC EIPLATOR MODEL NO. 101

Applicant Electronic Depilatory, Inc.

K-Number K771575

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EFQ 1977-09-06

LAPAROTOMY SPONGES

Applicant Surgilite Intl., Inc.

K-Number K771531

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DWJ 1977-09-06

AQUAMATIC K-MODULE MODEL K-20

Applicant Gorman Rupp Industries

K-Number K771537

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GEI 1977-09-06

DISP. GROUND PLATE

Applicant Edward Weck, Inc.

K-Number K771330

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GEI 1977-09-06

PATIENT GROUNDING CABLES

Applicant Edward Weck, Inc.

K-Number K771332

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MMK 1977-09-06

PROTECTOR

Applicant Richard-Allan Medical Ind., Inc.

K-Number K771611

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EBF 1977-09-06

NIMETICAP

Applicant Espe GmbH (Us)

K-Number K771654

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GEI 1977-09-06

CONDUCTIVE ELECTRODE GEL

Applicant Edward Weck, Inc.

K-Number K771331

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DXN 1977-09-06

ARTEOIAL TONOMETER ML-105

Applicant Nicolet Biomedical Instruments

K-Number K771449

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GEN 1977-09-06

COPE LUNG FORCEPS #305-218

Applicant J. Jamner Surgical Instruments, Inc.

K-Number K771624

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