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

MMK 1979-04-12

PROTECTOR II

Applicant Richard-Allan Medical Ind., Inc.

K-Number K790661

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CZP 1979-04-12

ANTISERUM, HUMAN, IGA

Applicant Kent Laboratories, Inc.

K-Number K790703

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GEI 1979-04-12

ELECTRODE, MODEL E7504 PREP II

Applicant Valleylab, Inc.

K-Number K790296

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DTL 1979-04-12

ADAPTERS-Y-TYPE

Applicant Dlp, Inc.

K-Number K790563

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GEI 1979-04-12

CIMARRON 1000 OR 1000-2

Applicant Cimarron Instruments, Inc.

K-Number K790293

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DAO 1979-04-12

ANTISERUM TO HUMAN IGM

Applicant Kent Laboratories, Inc.

K-Number K790705

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DTL 1979-04-12

ADAPTER-STRAIGHT

Applicant Dlp, Inc.

K-Number K790564

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DEW 1979-04-12

ANTISERUM TO HUMAN IGG

Applicant Kent Laboratories, Inc.

K-Number K790704

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GOL 1979-04-12

CORDIA T

Applicant Cordis Corp.

K-Number K790212

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GCO 1979-04-12

DELTA-ROL

Applicant Johnson & Johnson Professionals, Inc.

K-Number K790340

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FTY 1979-04-12

SURGICAL RULER

Applicant Richard-Allan Medical Ind., Inc.

K-Number K790660

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KWP 1979-04-12

KNEE COMPRESSION HOOK SYSTEM

Applicant Zimmer, Inc.

K-Number K790465

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