Medical Device Manufacturer · US , Sturbridge , MA

Luxtec Corp. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1986

Recent clearances: LUXSCOPE, TENOSCOPE, TENOSNARE

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Luxtec Corp. Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Jan 09, 1987

SPECULUM, VAGINAL, METAL FIBEROPTIC

Obstetrics & Gynecology · 29d