FLUROPERM 60-OK, PARAGON HDS-OK— 510(k) K000224
UnknownParagon Vision Sciences
FDA 510(k) clearance K000224 for FLUROPERM 60-OK, PARAGON HDS-OK, Unknown on 2000-04-17. Applicant: Paragon Vision Sciences. Device class: 2.
Clearance details
- Applicant
- Paragon Vision Sciences
- Product code
- Code MUW
- Device class
- Class 2
- Regulation
- 21 CFR 886.5916
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Mesa, AZ, US
Recent devices under product code MUW
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- K160859 — OPTIMUM GP OK Daily Wear Contact Lens (roflufocon D & E)
- K010109 — FLUOROPERM 151-OK, PARAGON HDS 100-OK
- K003933 — BOSTON EQUALENS II (OPRIFOCON A) CONTACT LENS FOR ORTHOKERATOLGY
- K973697 — AIRPERM (SIFLUFOCON A) RIGID GAS PERMEABLE OK CONTACT LENSES FOR DAILY WEAR ORTHOKERATOLOGY
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.