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

GDO 1979-10-17

BAYONET HEIFETZ CLIP APPLIERS

Applicant Edward Weck, Inc.

K-Number K791845

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DEW 1979-10-17

ANTISERUM TO HUMAN IMMUNOGLOBULINS

Applicant Icl Scientific

K-Number K791824

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LCP 1979-10-17

A-GENT GLYCOSPEC

Applicant Abbott Laboratories

K-Number K791642

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DLR 1979-10-17

HI-M-TEST MORPHINE

Applicant Technam, Inc.

K-Number K791551

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DLP 1979-10-17

CENTRIA PHENYTOIN RIA TEST SET

Applicant Ventrex Laboratories, Inc.

K-Number K791896

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DZI 1979-10-17

MONOJECT ENDOSSEOUS DENTAL IMPLANT TOOL

Applicant Sherwood Medical Co.

K-Number K791326

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NAB 1979-10-17

HAND TOWEL

Applicant Procter & Gamble Mfg. Co.

K-Number K791926

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FSM 1979-10-17

CENTRAL VENOUS CATHETER DRESSING TRAY

Applicant Ascep, Inc.

K-Number K791887

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DFT 1979-10-17

LANCER L-INA ANTI-IGM

Applicant Sherwood Medical Co.

K-Number K791402

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EFQ 1979-10-17

CATHETER CARE KIT REORDER 7940&7941

Applicant Ascep, Inc.

K-Number K791888

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DEW 1979-10-17

LANCER L-INA ANTI-IGG

Applicant Sherwood Medical Co.

K-Number K791403

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CGX 1979-10-17

CREATININE DIAG. REAGENT PICRIC ACID

Applicant Connecticut Diagnostics, Ltd.

K-Number K791994

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