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

EBF 1980-05-20

PRISMA-FILL

Applicant Dentsply Intl.

K-Number K801092

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EHP 1980-05-20

VACUDENT LUMIX 65

Applicant Vacudent Sales Corp.

K-Number K800574

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IKD 1980-05-20

R2 ESU CABLE-ADAPTER MODELS 160,161

Applicant R2 Corp.

K-Number K800934

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FYC 1980-05-20

STERILE ISOLATION GOWN

Applicant Medspec Corp.

K-Number K801069

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FKQ 1980-05-20

MOD. DM-356 IPS INTERFACE MODULE

Applicant Extracorporeal Medical Specialities, Inc.

K-Number K800771

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DSK 1980-05-20

PRESSURE MONITOR, MODEL 1131B

Applicant American Optical Corp.

K-Number K801110

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GEN 1980-05-20

STRAITH CHISEL FORCEPS

Applicant Surgical Technology Laboratories, Inc.

K-Number K801075

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IWZ 1980-05-20

KODAK EKTASPEED DENTAL X-RAY FILM

Applicant Eastman Kodak Company

K-Number K800901

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GEI 1980-05-20

VALLEYLAB RETURN ELECTRODE MONITOR

Applicant Valleylab, Inc.

K-Number K801153

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JOT 1980-05-20

R2 ELECTROSURG. RETURN ELECT. #225ETC.

Applicant R2 Corp.

K-Number K800933

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KKX 1980-05-20

STERILE DRAPE 17X18 CODE D-6A

Applicant Veratex Corp.

K-Number K801032

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KKX 1980-05-20

BOUNDARY EXTREMITY DRAPE

Applicant Procter & Gamble Mfg. Co.

K-Number K801132

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