Koven Technology, Inc.
Koven Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2021, with 1 FDA device recall on record.
Top product codes for Koven Technology, Inc.
FDA recalls by Koven Technology, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Koven Technology, Inc.
- K201114 — Bidop 7
- K153762 — Smartdop XT6
- K143332 — Fast Sphyg by Koven
- K131623 — SMARTDOP XT
- K080178 — VALVULOTOME BY KOVEN
- K050601 — SMARTDOP 45 VASCULAR DOPPLER
- K031931 — ECHO SOUNDER EX-101EX 8 MHZ
- K031504 — ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX
- K023143 — ECHO SOUNDER, ES-102EX
- K010452 — BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T
- K982986 — TUBING BLOOD FLOW METER MODEL NUMBER HD-800
- K961817 — B SMART MODEL 1
- K963274 — V-LINK 3.2 FOR WINDOWS
- K951449 — MODEL KM-25
- K954397 — BIDIRECTIONAL DOPPLER W/WAVEFORM DISPLAY
- K935994 — PW DOPPLER VASCULAR PROBES
- K942613 — SMARTDOP 30 BI-DIRECTIONAL BLOOD FLOW DETECTOR
- K934638 — REUSABLE CW DOPPLER PROBES: MODELS P8M05S8A, P8M05N5A, & LCW-8
Data sourced from openFDA. This site is unofficial and independent of the FDA.