OMNIPATCH— 510(k) K900941
Substantially EquivalentEye Garter Company, Inc.
FDA 510(k) clearance K900941 for OMNIPATCH, Substantially Equivalent on 1990-05-21. Applicant: Eye Garter Company, Inc.. Device class: 1.
Clearance details
- Applicant
- Eye Garter Company, Inc.
- Product code
- Code HOY
- Device class
- Class 1
- Regulation
- 21 CFR 886.4750
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Recent devices under product code HOY
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