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) Regulatory Record - 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

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