Microvena Corp.
Microvena Corp. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1999.
Top product codes for Microvena Corp.
Recent clearances by Microvena Corp.
- K991898 — ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE
- K991194 — MODIFICATION TO ULTRA-SELECT GUIDEWIRE
- K982657 — AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100
- K970668 — THE AMPLANTZ GOOSE NECK MICROSNARE
- K972511 — AMPLATZ GOOSE NECK SNARE KIT/ CATHETER
- K971984 — AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200)
- K954642 — HYDRO-SELECT GUIDEWIRE
- K954205 — THE AMPLATZ THROMBECTOMY DEVICE
- K955304 — CRICKET
- K952860 — THE NINER NITINOL GUIDEWIRE
- K946356 — M-PATH NITINOL GUIDEWIRE
- K925439 — MICROSNARE
- K922060 — .25' ULTRA-SELECT GUIDEWIRE
- K914046 — THE BIG EASY Y-ADAPTER
- K910280 — ULTRA-SELECT PTCA GUIDEWIRE
- K901502 — AMPLATZ GOOSE-NECK SNARE
- K900657 — UNIVERSAL DELIVERY SYSTEM CATHETER
- K896096 — SOLOSTICK (AMPLATZ DILATOR NEEDLE)
Data sourced from openFDA. This site is unofficial and independent of the FDA.