MICRO-MITT— 510(k) K830821
Substantially EquivalentCooperVision, Inc.
FDA 510(k) clearance K830821 for MICRO-MITT, Substantially Equivalent on 1983-04-27. Applicant: CooperVision, Inc.. Device class: 1.
Clearance details
- Applicant
- CooperVision, Inc.
- Product code
- Code FXP
- Device class
- Class 1
- Regulation
- 21 CFR 878.4040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Southampton, GB
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Data sourced from openFDA. This site is unofficial and independent of the FDA.