Teknar, Inc.
Teknar, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1990.
Top product codes for Teknar, Inc.
Recent clearances by Teknar, Inc.
- K903666 — OPHTHASONIC A/P III
- K896038 — B-SCAN 10 MHZ PROBE
- K896150 — IMAGE 2000 SYSTEM, IMAGING, ULTRA-SONIC
- K891777 — PRO-CUT BIOPSY NEEDLE
- K883965 — PROBE, IMAGING, ULTRASONIC, MECHANICAL SECTOR
- K881850 — TEKNAR PERCU-SCAN
- K881605 — BIOPSY GUIDE
- K880659 — TEKNAR PROSCAN ACCESSORY PROBE
- K871536 — OPHTHASONIC A-SCAN/ B-SCAN
- K864807 — TEKNAR PROSCAN(TM)
- K860757 — OPHTHASONIC A-SCAN
- K850116 — BETASONIC III
- K834539 — AXIPAC II
- K830474 — IV STAND
- K822900 — FISCH DRILL PUMP
- K823011 — VC III
- K810697 — AXISONIC II
- K801314 — VOCON MODEL VC526
Data sourced from openFDA. This site is unofficial and independent of the FDA.