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

N/A 1983-01-21

LATEX PENROSE TUBING

Applicant American Hospital Supply Corp.

K-Number K822755

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ESD 1983-01-21

RCI EARMATE

Applicant Rci, Inc.

K-Number K823089

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JYO 1983-01-21

KNIFE BLADE TIP

Applicant Treace Medical, Inc.

K-Number K823911

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GGP 1983-01-21

VON WILLEBRAND FACTOR ASSAY

Applicant General Diagnostics

K-Number K823453

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ILH 1983-01-21

FINGER EXTENSION SPLINT

Applicant Fred Sammons, Inc.

K-Number K823647

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GZJ 1983-01-21

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL

Applicant Medtronic Vascular

K-Number K823742

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KNO 1983-01-21

VELCRO STRAPS TO HOLD ARM TO WHEELCHAIR

Applicant Fred Sammons, Inc.

K-Number K823645

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ION 1983-01-21

BACK ON TRACK INVERSION THERAPY & EXER

Applicant Lossing Orthopedic, Inc.

K-Number K823236

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IKX 1983-01-21

BATH TUB SAFETY BAR

Applicant Fred Sammons, Inc.

K-Number K823640

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IOD 1983-01-21

SURGICAL TUBING

Applicant Fred Sammons, Inc.

K-Number K823648

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JPI 1983-01-21

MICRO-HEMATOCRIT CENTRIFUGE 335/336

Applicant Fisher Scientific Co., LLC

K-Number K823558

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JPH 1983-01-21

ERYTHROCYTE & STAND SEDIMENT. RATE TUBE

Applicant Cordis Corp.

K-Number K823761

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