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

JIS 1983-02-28

LITHIUM DILUENT

Applicant Shaban Mfg. Co.

K-Number K830283

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GEY 1983-02-28

RICHARDS INTRA-ARTICULAR SHAVER BLADES

Applicant Richard'S Medical Equip., Inc.

K-Number K830153

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DWD 1983-02-28

VEINPREP VEIN GRAFT PREP. KIT A277723

Applicant Atrium Medical Corp.

K-Number K830150

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FPA 1983-02-25

SECURA SET VOLUME LIMITING SET

Applicant Diatek, Inc.

K-Number K830448

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CIN 1983-02-25

ALKALINE PHOSPHATES ISOENZYME SUBSTRATE

Applicant Corning Medical & Scientific

K-Number K830118

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JJE 1983-02-25

STRATUS FLUOROMETRIC ENZYME IMMUN0-

Applicant American Hospital Supply Corp.

K-Number K830301

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DBF 1983-02-25

TANDEM-E -FER IMMUNOENZYMETRIC KIT

Applicant Hybritech, Inc.

K-Number K823871

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CDT 1983-02-25

TRIGLYCERIDE DIAGNOSTIC KIT

Applicant Sclavo, Inc.

K-Number K830288

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DHB 1983-02-25

INHALANT PROFILE-ALLERGEN-SPECIFIC IGE

Applicant Mast Immunosystems

K-Number K823593

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HIS 1983-02-24

SEMINAL COLLECTION DEVICE

Applicant Health Development Corp.

K-Number K823937

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HGP 1983-02-24

MULTI-PRONG FETAL SCALP ELECTRODE

Applicant Kontron Instruments, Inc.

K-Number K822584

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FKX 1983-02-24

NON-STERILE PERITONEAL ACCESS CATHET-

Applicant Evermed, Inc.

K-Number K830257

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