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

KYX 1980-03-12

SYRINGE TIP CONNECTOR

Applicant Burron Medical Products, Inc.

K-Number K800437

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FKQ 1980-03-12

DMS 3000

Applicant Renal Care Corp.

K-Number K792252

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FSM 1980-03-10

MICRESURGICAL TRAY, SM.,MED., & LG.

Applicant Edward Weck, Inc.

K-Number K800367

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KTZ 1980-03-10

PARKE-DAVIS TOTAL KNEE PROSTHESIS

Applicant Warner-Lambert Co.

K-Number K800363

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FRN 1980-03-10

3M SMALL VOLUME INFUSTION (SVI) SYSTEM

Applicant 3M Company

K-Number K792050

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ERA 1980-03-10

EARSCOPE

Applicant Nash & Assoc.

K-Number K800365

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CAF 1980-03-10

0.9% SODIUM CHLORIDE SOL./RESP. THERAPY

Applicant Abbott Laboratories

K-Number K800295

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HBT 1980-03-10

DOUBLETIME 2-TIPPED APPLIERS FOR HEMOCLI

Applicant Edward Weck, Inc.

K-Number K800318

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DXN 1980-03-10

MICRONTA BP-1 ELECTRONIC B/P TESTER

Applicant Tandy Corp.

K-Number K800225

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HPL 1980-03-10

AMBLYOPIA TRAINER

Applicant Life-Tech Instruments, Inc.

K-Number K800112

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ETP 1980-03-10

HYGROTHERM

Applicant Jedmed Instrument Co.

K-Number K800443

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CAF 1980-03-10

0.45% SODIUM CHLORIDE SOL./RESP. THERAPY

Applicant Abbott Laboratories

K-Number K800294

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