DW232 #31— 510(k) K932774
Substantially EquivalentInvoclar North America, Inc.
FDA 510(k) clearance K932774 for DW232 #31, Substantially Equivalent on 1993-10-20. Applicant: Invoclar North America, Inc.. Device class: 2.
Clearance details
- Applicant
- Invoclar North America, Inc.
- Product code
- Code EJT
- Device class
- Class 2
- Regulation
- 21 CFR 872.3060
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Amherst, NY, US
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