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

DRX 1983-04-28

PENCIL SKIN ABRADER

Applicant Ndm Corp.

K-Number K830663

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FSA 1983-04-28

MARTIN PELVIC LIFT

Applicant Martin Pelvic Lift Co.

K-Number K823206

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CAF 1983-04-28

SINGLE USE NEBULIZER, ADJUST. AIR-

Applicant Airlife, Inc.

K-Number K830895

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LKG 1983-04-28

VENTRICULAR ACCESS SYSTEM

Applicant American Heyer Schulte

K-Number K823790

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N/A 1983-04-28

TRANSPARENT X-RAY COMPENSATION FILTER

Applicant Victoreen, Inc.

K-Number K837245

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KDI 1983-04-28

HEMO-PROCESSING SYSTEM

Applicant Sartorius Filters, Inc.

K-Number K830487

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BTR 1983-04-28

SURGITEK ENDOTRACHEAL TUBE, LASER RESIS

Applicant Medical Engineering Corp.

K-Number K823757

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KQQ 1983-04-28

ASEPTIC FLUID TRANSFER SYSTEM

Applicant Steridoc Corp.

K-Number K830811

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HXY 1983-04-28

ANDREWS REMOTE CHUCK DRILL

Applicant Orthopedic Systems, Inc.

K-Number K831043

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DYB 1983-04-28

FRENCH PERCUTANEOUS SHEATH INTRODUCER

Applicant Norton Performance Plastics Corp.

K-Number K830813

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CAF 1983-04-28

PREFILLED RESPIRATORY THERAPY VIAL

Applicant Automatic Liquid Packaging, Inc.

K-Number K830943

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JSM 1983-04-28

I/A KIT

Applicant Staar Surgical Co.

K-Number K831159

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