Medical Device Manufacturer · US , Mchenry , IL

Clinical Technology Corp. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1982

Total

Cleared

Denied

Clinical Technology Corp. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1982 to 1994. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Clinical Technology Corp.

12 devices

1-12 of 12

General Hospital · 351d

Cleared Feb 18, 1988

BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000

K880166 · LFL

General & Plastic Surgery · 35d

Cleared Sep 01, 1987

BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)

K872705 · GEI

General & Plastic Surgery · 56d

Cleared Nov 10, 1986

BOVIE ULTRASONIC SURGICAL SYSTEM

K855138 · LBK

Neurology · 322d

Cleared May 02, 1986

ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES

K854231 · GEI

General & Plastic Surgery · 193d

Cleared Sep 05, 1985

STERI-GRIP

K853507

General & Plastic Surgery · 15d

Cleared Aug 19, 1985

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN

K852986 · LCP

Hematology · 35d

Cleared Feb 21, 1985

BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)

K844565 · GEI

General & Plastic Surgery · 90d

Cleared Apr 13, 1984

SICKLE-STAT HEMOGLOBIN S SCREEN KIT

K841272 · GHM

Hematology · 17d

Cleared Mar 09, 1983

URINARY BLADDER TEMP. SENSOR #81-003

K823077 · FLL

General Hospital · 141d

Cleared Jan 22, 1982

DISPOSABLE ARTHROSCOPY CANNULA SET

K813000 · LXH

Orthopedic · 88d

Clinical Technology Corp. - FDA 510(k) Cleared Devices

Filters