PARAGON LENS VIAL— 510(k) K993487
Substantially EquivalentParagon Vision Sciences
FDA 510(k) clearance K993487 for PARAGON LENS VIAL, Substantially Equivalent on 1999-12-22. Applicant: Paragon Vision Sciences. Device class: 2.
Clearance details
- Applicant
- Paragon Vision Sciences
- Product code
- Code LRX
- Device class
- Class 2
- Regulation
- 21 CFR 886.5928
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mesa, AZ, US
Recent devices under product code LRX
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- K231123 — Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more
- K173538 — Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc
More clearances from Paragon Vision Sciences
view all- K180172 — FluoroPerm 30 & Paragon Thin (paflufocon C) RGP contact lenses with Tangible Hydra-PEG +3 more
- K120996 — FLUOROPERM 30 PARAGON HDS FLUOROPERM 60 PARAGON HDS 100 FLUOROPERM 92 FLUOROPERM 151 PARAGON THIN
- K082799 — HDS HI 1.54
- K070637 — FLUOROPERM 92, 60, 30 AND 151 AND PARAGON HDS, HDS 100 AND THIN RIGID GAS PERMEABLE CONTACT LENSES
- K052983 — FLUOROPERM 151 (PAFLUFOCON D) AND PARAGON HDS 100 (PAFLUFOCON D) RIGID GAS PERMEABLE CONTACT LENSES
Data sourced from openFDA. This site is unofficial and independent of the FDA.