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

FKQ 1982-04-16

GAMBRO LUNDIA 10 3N PARALLEL FLOW DIAL

Applicant Gambro, Inc.

K-Number K820769

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JSE 1982-04-16

CULTURE MEDIA, MULTIPLE BIOCHEMICAL

Applicant Blue Ridge Media Co.

K-Number K820841

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CGS 1982-04-16

SERALYZER CK REAGENT STRIPS

Applicant Miles Laboratories, Inc.

K-Number K820880

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DTL 1982-04-15

NORTON MANIFOLD

Applicant Norton Performance Plastics Corp.

K-Number K820864

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N/A 1982-04-15

SYSTEM 287 SCANNER

Applicant Diagnostic Sonar USA

K-Number K827209

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HRX 1982-04-15

CANNUOATED TROCHAR

Applicant The Anspach Effort, Inc.

K-Number K820776

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BYJ 1982-04-15

MARK III OXYGEN WALKER SYSTEM

Applicant Union Carbide Corp.

K-Number K820836

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BZG 1982-04-15

AUTOSPIROMETER HI-498

Applicant Medical Equipment Designs, Inc.

K-Number K820599

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LOS 1982-04-15

MARQUETTE OPTION II ECG ANALYSIS COMPUT

Applicant Marquette Electronics, Inc.

K-Number K820885

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DRT 1982-04-15

CARDIAC MONITOR - RATE ALARM

Applicant Hewlett-Packard Co.

K-Number K820825

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GCX 1982-04-15

PLEURAL DRAINAGE RESERVOIR

Applicant Innovative Surgical Products, Inc.

K-Number K820765

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CED 1982-04-15

PHOSPHORUS IL

Applicant American Monitor Corp.

K-Number K820832

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