TRI*STAR— 510(k) K930711
Substantially EquivalentLight Technology Systems
FDA 510(k) clearance K930711 for TRI*STAR, Substantially Equivalent on 1993-07-30. Applicant: Light Technology Systems. Device class: 2.
Clearance details
- Applicant
- Light Technology Systems
- Product code
- Code FSS
- Device class
- Class 2
- Regulation
- 21 CFR 878.4580
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Van Nuys, CA, US
Recent devices under product code FSS
view all- K091246 — ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)
- K003489 — NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8
- K984124 — AESCULAP XENON LIGHT SOURCE
- K981962 — CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE
- K981821 — VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.