WIRONTOM CLASP WIRE— 510(k) K901257
Substantially EquivalentIvoclar North America, Inc.
FDA 510(k) clearance K901257 for WIRONTOM CLASP WIRE, Substantially Equivalent on 1990-04-25. Applicant: Ivoclar North America, Inc.. Device class: 1.
Clearance details
- Applicant
- Ivoclar North America, Inc.
- Product code
- Code EJW
- Device class
- Class 1
- Regulation
- 21 CFR 872.3285
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
Recent devices under product code EJW
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