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 1979-06-01

VITALITH S 3000 SERIES

Applicant Vitatron Medical BV

K-Number K790666

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KPE 1979-06-01

CAP, TAMPER PROOF PLASTIC

Applicant Acacia, Inc.

K-Number K782113

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HGM 1979-06-01

FETASONDE MODEL 2108

Applicant Roche Medical Electronics, Inc.

K-Number K790761

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DRX 1979-06-01

ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA

Applicant Physio-Control Corp.

K-Number K791003

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DRX 1979-06-01

ECG ELECTRODES, PEDIATRIC-FOAM TAPE

Applicant Physio-Control Corp.

K-Number K791002

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FMQ 1979-06-01

TECNOL BODY HOLDER

Applicant Tecnol New Jersey Wound Care, Inc.

K-Number K790699

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FPB 1979-06-01

ULTIPOR SOLUTION CONTAINER FILTER

Applicant Pall Biomedical Products Co.

K-Number K790879

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FRN 1979-06-01

MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU

Applicant Vickers America Medical Corp.

K-Number K790945

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KME 1979-06-01

AUTO TRAUMA KIT

Applicant Marshall Electronics, Inc.

K-Number K790411

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FAP 1979-06-01

BROWNE MODEL CF-1 AND CF-1G

Applicant Browne Corp.

K-Number K790754

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KOD 1979-06-01

TOUCHLESS TM FOLEY CATHETER KIT

Applicant Diamed Division Ill. Tool Works, Inc.

K-Number K790728

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FRN 1979-06-01

ALARM

Applicant Maddak, Inc.

K-Number K790559

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