CONTACT LENSES METRO-G 3X (HIOXIFILCON B)— 510(k) K964902
Substantially EquivalentMetro Optics of Austin, Inc.
FDA 510(k) clearance K964902 for CONTACT LENSES METRO-G 3X (HIOXIFILCON B), Substantially Equivalent on 1997-03-11. Applicant: Metro Optics of Austin, Inc.. Device class: 2.
Clearance details
- Applicant
- Metro Optics of Austin, Inc.
- Product code
- Code LPL
- Device class
- Class 2
- Regulation
- 21 CFR 886.5925
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rosewell, GA, US
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More clearances from Metro Optics of Austin, Inc.
view all- K233221 — Metro Soft, Silicone Hydrogel Daily Wear Soft Contact Lens (efrofilcon A)
- K100244 — METRO SOFT
- K080512 — REVITALEYES, POST-SURGICAL SOFT DAILY WEAR CONTACT LENS (HIOXIFILCON B) CLEAR AND BLUE VISIBILITY TINT
- K031532 — SATUREEYES II (ACOFILCON A), (ACOFILCON B) & (TETRAFILCON A) SOFT CONTACT LENS FOR DAILY WEAR
- K001620 — METROFOCAL TORIC (POLYMACON) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBILITY TINT, LATHE-CUT FROM LEN
Adverse events under product code LPL
product code LPL- Injury
- 988
- Other
- 4
- Total
- 992
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.