KERAMAIL— 510(k) K915653
Substantially EquivalentWilde-USA, Inc.
FDA 510(k) clearance K915653 for KERAMAIL, Substantially Equivalent on 1993-04-08. Applicant: Wilde-USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Wilde-USA, Inc.
- Product code
- Code EIH
- Device class
- Class 2
- Regulation
- 21 CFR 872.6660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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