CODERE-DURETTE ORBITAL FLOOR IMPLANT— 510(k) K900927
Substantially EquivalentOculo Plastik, Inc.
FDA 510(k) clearance K900927 for CODERE-DURETTE ORBITAL FLOOR IMPLANT, Substantially Equivalent on 1990-05-15. Applicant: Oculo Plastik, Inc.. Device class: 2.
Clearance details
- Applicant
- Oculo Plastik, Inc.
- Product code
- Code HQX
- Device class
- Class 2
- Regulation
- 21 CFR 886.3340
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Montreal, Quebec Canada, CA
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