WOODLYN LIGHTWEIGHT TRIAL FRAME— 510(k) K841768
Substantially EquivalentWoodlyn, Inc.
FDA 510(k) clearance K841768 for WOODLYN LIGHTWEIGHT TRIAL FRAME, Substantially Equivalent on 1984-06-01. Applicant: Woodlyn, Inc.. Device class: 1.
Clearance details
- Applicant
- Woodlyn, Inc.
- Product code
- Code HPA
- Device class
- Class 1
- Regulation
- 21 CFR 886.1415
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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