TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025— 510(k) K003036
Substantially EquivalentRetinalabs.Com
FDA 510(k) clearance K003036 for TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025, Substantially Equivalent on 2000-12-22. Applicant: Retinalabs.Com. Device class: 1.
Clearance details
- Applicant
- Retinalabs.Com
- Product code
- Code KYG
- Device class
- Class 1
- Regulation
- 21 CFR 886.4360
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
Recent devices under product code KYG
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view all- K000418 — PDT DOSECALCULATOR, MODEL 80000
- K000457 — VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES
- K000416 — TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001
- K000420 — SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003
Data sourced from openFDA. This site is unofficial and independent of the FDA.