LENS— 510(k) K821897
Substantially EquivalentMortan, Inc.
FDA 510(k) clearance K821897 for LENS, Substantially Equivalent on 1983-01-05. Applicant: Mortan, Inc.. Device class: 1.
Clearance details
- Applicant
- Mortan, Inc.
- Product code
- Code KYG
- Device class
- Class 1
- Regulation
- 21 CFR 886.4360
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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