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

KOD 1980-10-31

FOLEY CATHETER

Applicant Abco Dealers, Inc.

K-Number K802516

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DBI 1980-10-31

GOAT ANTI-HUMAN COMPLEMENT C4

Applicant Protos Laboratories

K-Number K802196

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FLK 1980-10-31

FERTILITY AWARENESS METHOD KIT

Applicant Telesis Corp.

K-Number K801791

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FKK 1980-10-31

FLOWCLAMP CAT.#1011 & 1012

Applicant Pollak (Intl.), Ltd.

K-Number K802009

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DKC 1980-10-31

EMIT-STM ETHYL ALCOHOL URINE CONTROLS

Applicant Syva Co.

K-Number K802618

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KSR 1980-10-31

PLASMAPOOLER

Applicant North American Biologicals, Inc.

K-Number K801219

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HRY 1980-10-31

RANAWAT ESF TOTAL CONDYLAR KNEE

Applicant Howmedica Corp.

K-Number K802446

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FNY 1980-10-31

BASIN PACK

Applicant Texas Medical Products, Inc.

K-Number K802538

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HHI 1980-10-31

UTERINE VACUM ASPIRATING CURRETTE

Applicant American Hospital Supply Corp.

K-Number K802360

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CAP 1980-10-31

3MP-7 SCANNER RESPIRATORY MONITOR

Applicant Bird Products Corp.

K-Number K802565

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DEW 1980-10-31

GOAT ANTI-HUMAN IGG GAMMA CHAIN SPECIFIC

Applicant Protos Laboratories

K-Number K802257

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CGI 1980-10-31

ESTRIOL-SQUIBB RIA KIT

Applicant E. R. Squibb & Sons, Inc.

K-Number K802455

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