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 1979-05-25

GENERATOR, 16 SERIES, MODIFIED TOP CAP

Applicant Telectronics, Inc.

K-Number K790868

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DBM 1979-05-25

TEST KIT, IIF-AMA

Applicant Medica Corp.

K-Number K790295

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BSJ 1979-05-25

ACCUTRON POLLUTION REDUCER

Applicant Parker Laboratories, Inc.

K-Number K790638

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DXQ 1979-05-25

DISPOSA-CUF

Applicant Crest Medical Equipment

K-Number K790810

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DTL 1979-05-25

PURGE LINE UNIT

Applicant Surgikos, Inc.

K-Number K790804

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DTB 1979-05-25

MEDTRONIC MODELS 6907/6901

Applicant Medtronic Vascular

K-Number K790766

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IPF 1979-05-25

EGS MODEL 300

Applicant Alfred V. Greco

K-Number K790847

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GKT 1979-05-24

TERUMO IMUGARD

Applicant Terumo America, Inc.

K-Number K790105

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JIW 1979-05-23

CENTRIFICHEM FILTER CALIBRATION SET

Applicant Union Carbide Corp.

K-Number K790643

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CHH 1979-05-23

REAGENT SYSTEM #350HDL, SIGMA PROCEDURE

Applicant Sigma Chemical Co.

K-Number K790760

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KSG 1979-05-23

DADE LOW IONIC STRENGTH SOLUITION (LISS)

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K790776

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KSN 1979-05-23

IMMU-TEK AUTOMATIC CENTRIFUGE

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K790767

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