Luxtec Corp.
Luxtec Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1997.
Top product codes for Luxtec Corp.
Recent clearances by Luxtec Corp.
- K973193 — LUXSCOPE
- K970642 — TENOSCOPE
- K970562 — TENOSNARE
- K950960 — REDDY ILLUMINATOR
- K895248 — IMS5000 ILLUMINATED LOUPES
- K890716 — LUXTEC ACO SERIES 4000 LIGHT SOURCE
- K864387 — LUXTEC FIBEROPTIC CABLES
- K864382 — FRAZIER SUCTION TUBE
- K864383 — LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS
- K864385 — LUXTEC LIGHT SOURCES
- K864865 — SPECULUM, VAGINAL, METAL FIBEROPTIC
- K864381 — LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEM
- K864380 — LUTEX HEADLIGHT SYSTEMS
- K864384 — LUXTEC RETRACTORS, LUXTEC SPECIALTY RETRACTORS
- K864386 — LUXTEC LOUPES FOR SURGICAL VISION
Data sourced from openFDA. This site is unofficial and independent of the FDA.