CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE— 510(k) K981962
Substantially EquivalentCuda Products Co.
FDA 510(k) clearance K981962 for CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE, Substantially Equivalent on 1998-08-18. Applicant: Cuda Products Co.. Device class: 2.
Clearance details
- Applicant
- Cuda Products Co.
- 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
- Jacksonville, FL, 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
- K981821 — VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR
- K981469 — CERMAX300 LIGHTSOURCE
More clearances from Cuda Products Co.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.