Satelec
Satelec holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2011.
Top product codes for Satelec
Recent clearances by Satelec
- K110379 — AIR-N-GO
- K100410 — PIEZOELECTRIC SYSTEM
- K091331 — PIEZOTOME 2
- K091252 — IMPLANT CENTER 2
- K082116 — HEMOSTASYL PASTE
- K072181 — MINI LED AUTOFOCUS
- K071965 — I-SURGE
- K060275 — PIEZOTOME
- K060274 — PIEZOTOME
- K053328 — BIOSPLINT SPLINTING RIBBON
- K050895 — SURPASSON P5 NEWTRON
- K042787 — IS 40 MICROMOTOR
- K040529 — COCOON HYGIENIST
- K040808 — MINI L.E.D. OEM MODULE
- K033764 — SP NEWTRON MODULE
- K032465 — MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI
- K011001 — TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEM
- K000049 — SUNI MAX
- K972612 — DISSECTRON PORTABLE UNIT
- K972026 — SP4044 & SP4055 LUX MODULES
- K961735 — ACTA
- K961158 — SUPRASSON P5 BOOSTER
- K942139 — SUPRASSON P MAX
- K904067 — LASERSAT CO2
Data sourced from openFDA. This site is unofficial and independent of the FDA.