SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR— 510(k) K080193
Substantially EquivalentSynergeyes, Inc.
FDA 510(k) clearance K080193 for SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR, Substantially Equivalent on 2008-03-05. Applicant: Synergeyes, Inc.. Device class: 2.
Clearance details
- Applicant
- Synergeyes, Inc.
- Product code
- Code HQD
- Device class
- Class 2
- Regulation
- 21 CFR 886.5916
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rockville, MD, US
Recent devices under product code HQD
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More clearances from Synergeyes, Inc.
view all- K153714 — SynergEyes A&M (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes KC (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes PS (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes SiH (petrafocon A hem-larafilcon A) Hybrid Daily Wear Contact Lens, SynergEyes UltraHealth for Keratoconus (petrafocon A hem-larafilcon A) Hybrid Daily Wear Co
- K160938 — SynergEyes SiH with Hydra-PEG(petrafocon A hem-larafilcon A) Hybrid Daily Wear Lens
- K142510 — UltraHealth Hybrid Contact Lens for Keratoconus, UltraHealth Flat Cornea Hybrid Contact Lens
- K113586 — SYNERGEYES SIH (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENS
- K083921 — SYNERGEYES SIG (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENS
Data sourced from openFDA. This site is unofficial and independent of the FDA.