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

EBI 1983-06-08

VINYLAC PRESS-PACK DENTURE RESIN

Applicant Astron Dental Corp.

K-Number K831269

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EJT 1983-06-08

NEY-ORO 60

Applicant Deringer-Ney, Inc.

K-Number K831280

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ILP 1983-06-08

ADAPTIVE PENS & LAP DESK

Applicant Fred Sammons, Inc.

K-Number K831546

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DCN 1983-06-08

CRP-CHECK

Applicant Diagnostic Technology, Inc.

K-Number K831465

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DHB 1983-06-08

NEIN ALLERGEN DISC IN VAST VENTREX TEST

Applicant Ventrex Laboratories, Inc.

K-Number K831554

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JKA 1983-06-08

LIPOSOL

Applicant Quest Medical, Inc.

K-Number K830472

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HRX 1983-06-08

CRAFON ARTHROSCOPY LINES

Applicant Gambro, Inc.

K-Number K830673

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HQC 1983-06-08

ULTRAKIT

Applicant Staar Surgical Co.

K-Number K831172

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FPA 1983-06-08

SOLUTION ADMIN. SETS W/FLASHBALL

Applicant Travenol Laboratories, S.A.

K-Number K831311

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N/A 1983-06-08

ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS

Applicant New England Surgical Instrument Corp.

K-Number K831426

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JHI 1983-06-08

BHCG RIA KIT

Applicant Micromedic Systems

K-Number K831264

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JFB 1983-06-08

WEYLAND EXTENSION VIBRATOR

Applicant Medical Management Service, Inc.

K-Number K822413

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