Medical Device Manufacturer · US , Mchenry , IL

Gilford - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1981

Official Website

Total

Cleared

Denied

Gilford has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1981 to 1985. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Gilford Filter by specialty or product code using the sidebar.

Gilford is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gilford

10 devices

1-10 of 10

Cleared Sep 16, 1985

GILFORD IMMUNOGLOBULIN G REAGENT

K853465 · DEW

Immunology · 28d

Cleared Sep 16, 1985

GILFORD C3 COMPLEMENT REAGENT

K853466 · CZW

Immunology · 28d

Cleared Sep 16, 1985

GILFORD IMMUNOGLOBULIN A REAGENT

K853467 · CZP

Immunology · 28d

Cleared Sep 16, 1985

GILFORD C4 COMPLEMENT REAGENT

K853468 · DBI

Immunology · 28d

Cleared Sep 16, 1985

GILFORD IMMUNOGLOBULIN M REAGENT

K853469 · DFT

Immunology · 28d

Cleared Apr 29, 1985

GILFORD TRI-LEVEL ASSAYED IMMUNOLOGY CONTROL

Gilford - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gilford

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