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

FNJ 1981-09-23

GER 540, GER 541 MANUAL BED

Applicant G.W. Healthcare, Inc.

K-Number K812600

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EQH 1981-09-23

DALE COMBO TRACHEOSTOMY TUBE HOLDER

Applicant Dale Medical Products, Inc.

K-Number K812429

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KTQ 1981-09-23

RABBIT COMPLEMENT

Applicant Dutchland Laboratories, Inc.

K-Number K812522

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LER 1981-09-23

AMES TDA THEOPHYLLINE TEST

Applicant Miles Laboratories, Inc.

K-Number K812518

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DXY 1981-09-23

MEDTRONIC MODEL 2409

Applicant Medtronic Vascular

K-Number K812580

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DEW 1981-09-23

IMMUNOGL. FRCT. OF RABBIT ANTISER.-IGG

Applicant Dako Corp.

K-Number K812489

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CZP 1981-09-23

IMMUNOGL. FRCT. OF RABBIT ANTISER.-IGA

Applicant Dako Corp.

K-Number K812488

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DXY 1981-09-23

TELEMETRY DECODER

Applicant Intermedics, Inc.

K-Number K801339

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DCF 1981-09-23

IMMUNOGL. FRCT. OF RABBIT ANTISER.-ALBUM

Applicant Dako Corp.

K-Number K812496

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CAW 1981-09-21

MINI O2

Applicant Mountain Medical Equipment, Inc.

K-Number K812513

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LBH 1981-09-21

CAVITY VARNISH

Applicant Dentsply Intl.

K-Number K810913

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HNN 1981-09-21

KOI DIAMOND KNIFE

Applicant Koi, Inc.

K-Number K812450

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