Medical Device Manufacturer · US , Mchenry , IL

Teknar, Inc. - FDA 510(k) Cleared Devices

18 submissions · 17 cleared · Since 1980

Total

Cleared

Denied

Teknar, Inc. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1980 to 1990. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Teknar, Inc.

18 devices

1-18 of 18

IMAGE 2000 SYSTEM, IMAGING, ULTRA-SONIC

K896150 · IYO

Radiology · 87d

Cleared May 04, 1989

PRO-CUT BIOPSY NEEDLE

K891777 · FCG

Gastroenterology & Urology · 41d

Cleared Oct 05, 1988

PROBE, IMAGING, ULTRASONIC, MECHANICAL SECTOR

TEKNAR PROSCAN ACCESSORY PROBE

K880659 · IYO

Radiology · 57d

Cleared Aug 26, 1987

OPHTHASONIC A-SCAN/ B-SCAN

General & Plastic Surgery · 40d

Cleared Nov 08, 1982

VC III

K823011 · EPT

General & Plastic Surgery · 26d

Cleared Jul 13, 1981

AXISONIC II

K810697 · HDR

Obstetrics & Gynecology · 119d

Cleared Sep 09, 1980

VOCON MODEL VC526

K801314 · FSO

General & Plastic Surgery · 98d

Teknar, Inc. - FDA 510(k) Cleared Devices

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