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

HNY 1983-07-12

DISPOSABLE CYSTOTOME

Applicant CooperVision, Inc.

K-Number K831916

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KNT 1983-07-12

BROOKS SCLEROTHERAPY CUFF

Applicant Inmed Corp.

K-Number K823475

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HAW 1983-07-12

DAP II BIOPSY GUIDE

Applicant Rapid Machine & Tool Corp.

K-Number K830999

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BXB 1983-07-12

STRYKER LEG EXERCISER

Applicant Stryker Corp.

K-Number K831910

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FMI 1983-07-12

INTRADISCAL THERAPY NEEDLE

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K831610

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JDK 1983-07-12

BARD INTRAMEDULLARY PLUG

Applicant C.R. Bard, Inc.

K-Number K831128

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GAA 1983-07-12

TRU-CUT BIOPSY/ASPIRA-NEEDLE 2N2709

Applicant Travenol Laboratories, S.A.

K-Number K831392

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GQL 1983-07-07

INDIRECT FLUORO-KIT HSV

Applicant Clinical Sciences, Inc.

K-Number K830623

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N/A 1983-07-07

ACU-PUNCH

Applicant Acuderm, Inc.

K-Number K831635

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BTO 1983-07-07

ARGYLE SILICONE TRACHESTOMY TUBE W/LOW

Applicant Sherwood Medical Co.

K-Number K831720

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BSJ 1983-07-07

NON CONDUCTIVE ANESTHESIA FACEMASK

Applicant Vital Signs, Inc.

K-Number K831713

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FIQ 1983-07-07

HEMOCLAV VENOUS CATHETER

Applicant Exo, Inc.

K-Number K831801

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