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

ESD 1983-03-07

800 BLUE

Applicant Electone, Inc.

K-Number K830303

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ESD 1983-03-07

HEARING AID, #UE7-D

Applicant Unitron Industries, Inc.

K-Number K830402

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N/A 1983-03-07

ELDER PSORALITE, SERIES 43000

Applicant Elder Pharmaceuticals, Inc.

K-Number K837105

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JSJ 1983-03-07

LEGIONELLA SELECTIVE SUPPLEMENTS

Applicant Gibco Laboratories Life Technologies, Inc.

K-Number K830384

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JSG 1983-03-07

MINIATURE ION SELECTIVE ELECTRODES

Applicant Ionetics, Inc.

K-Number K830130

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ETD 1983-03-07

OTOLOGICAL VENTILATION TUBES-VARIOUS

Applicant Micromedics, Inc.

K-Number K830228

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GZJ 1983-03-07

AUTO-TENS MODEL III DUAL CHANNEL REPLACE

Applicant Cbc Corp.

K-Number K823466

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JXA 1983-03-07

DIPCHEX DIP-SLIDE CULTURE SYS

Applicant Granite Diagnostics, Inc.

K-Number K830252

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LFJ 1983-03-07

DOUBLE LUMEN SUBCLAVIAN CATHETER

Applicant Abbott Laboratories

K-Number K823135

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KHE 1983-03-07

FECAL OCCULT SLIDE TEST KIT

Applicant Cambridge Chemical Products, Inc.

K-Number K830223

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CFF 1983-03-07

PARAGON IMMUNOELECTROPHORESIS REAGENT

Applicant Beckman Instruments, Inc.

K-Number K823884

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BXN 1983-03-07

MYOGRAPH 2000

Applicant Prothia USA, Inc.

K-Number K830058

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