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

LCP 1981-01-16

SANDARE GLYCOHEMOGLOBIN PROCEDURE

Applicant Sandare Chemical Co., Inc.

K-Number K802832

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KRI 1981-01-16

DISPOSABLE CONNECTORS

Applicant Texas Medical Products, Inc.

K-Number K802542

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LGL 1981-01-16

ALPHA-THAL SCREEN 20 TEST KIT & 100 KIT

Applicant Isolab, Inc.

K-Number K801771

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DTL 1981-01-16

DISPOSABLE QUICK RELEASE PERFUSION ADAP

Applicant Texas Medical Products, Inc.

K-Number K802544

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DXQ 1981-01-16

ALP-KII

Applicant Martin'S Maine Exchange

K-Number K810008

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DTB 1981-01-16

PERM. ENDOCARDIAL UNIPOLAR WEDGE URETHAN

Applicant Daig Corp.

K-Number K802553

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CGS 1981-01-16

CREATINE KINASE REAGENT

Applicant Gilford Diagnostics

K-Number K803301

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JJT 1981-01-16

DUPONT 'ACA' CREATINE KINASE VERIFIERS

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K803305

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KRI 1981-01-16

DISPOSABLE PARALLEL Y CONNECTORS

Applicant Texas Medical Products, Inc.

K-Number K802541

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CFT 1981-01-16

PROLACTIN (125) RADIOIMMUNAOASSAY

Applicant Corning Medical & Scientific

K-Number K803273

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HGW 1981-01-16

FETAL BLOOD SAMPLING KIT MODEL 1560

Applicant Transidyne General Corp.

K-Number K810028

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GIM 1981-01-16

SYRINGE FOR BLOOD SAMPLING

Applicant The University of Chicago

K-Number K803182

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