Medical Device Manufacturer · US , Mchenry , IL

Concord Laboratories, Inc. - FDA 510(k) Cleared Devices

42 submissions · 38 cleared · Since 1976

Total

Cleared

Denied

Concord Laboratories, Inc. has 38 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 38 cleared submissions from 1976 to 1989.

Browse the FDA 510(k) cleared devices submitted by Concord Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Concord Laboratories, Inc.

42 devices

1-12 of 42

Cleared May 16, 1989

DRI-VENT ARTERIAL BLOOD SAMPLING KIT

K883840 · LKB

General Hospital · 246d

Cleared Jun 29, 1987

MECONIUM SUCTION CATHETER

K871825 · BSY

Anesthesiology · 49d

Cleared Jan 06, 1987

TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110

General & Plastic Surgery · 36d

Cleared Jan 10, 1986

SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH

K854601 · BSO

Anesthesiology · 53d

Cleared Nov 13, 1985

SUBCUTANEOUS TUNNELING NEEDLES & HANDLES

K854327 · GCB

General & Plastic Surgery · 16d

Cleared Jul 15, 1985

REGIONAL ANESTHESIA TRAYS

K851134 · CAZ

Anesthesiology · 116d

ARTERIAL BLOOD SAMPLING KITS

K841486 · CBT

Anesthesiology · 43d

Cleared Apr 05, 1984

PREFILLED PULSATOR SYRINGE

MID-STREAM URINE COLLECTION SETS

K840709

Gastroenterology & Urology · 46d

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Concord Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Concord Laboratories, Inc.

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