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

EFQ 1983-03-29

FLORET DRAIN/TRACHEOTOMY SPONGE

Applicant Ritmed, Inc.

K-Number K830265

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KOC 1983-03-29

C-DAK ARTIFICIAL KIDNEY

Applicant Cordis Corp.

K-Number K830729

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FOZ 1983-03-29

PRE VUE

Applicant Taut, Inc.

K-Number K830573

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GEI 1983-03-29

DISPERSIVE ELECTRODE

Applicant C.R. Bard, Inc.

K-Number K830545

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FKX 1983-03-29

ABBOTT PATIENT ASSIST DEVICE

Applicant Abbott Laboratories

K-Number K830766

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JTQ 1983-03-28

C.A.T. REAGENT KIT

Applicant Remel Co.

K-Number K830322

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LDG 1983-03-28

PHYSICIANS CHOICE SILICONE EAR PUTTY

Applicant Santa Barbara Medco, Inc.

K-Number K823921

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N/A 1983-03-28

CART

Applicant Medical Assoc. Intl., Inc.

K-Number K823925

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INQ 1983-03-25

PDB II

Applicant J.A. Gerber Therapeutical, Ltd.

K-Number K830289

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JQP 1983-03-25

CORNING 102 PRINTER

Applicant Corning Medical & Scientific

K-Number K830296

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KTT 1983-03-25

CORSTREN COMPRESSION TUBE & PLATE

Applicant Zimmer, Inc.

K-Number K830196

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N/A 1983-03-25

PHADEZYM B2 MICRO TEST 100

Applicant Pharmacia, Inc.

K-Number K830280

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