BAYSILEX— 510(k) K854106
Substantially EquivalentCutter Laboratories, Inc.
FDA 510(k) clearance K854106 for BAYSILEX, Substantially Equivalent on 1986-03-17. Applicant: Cutter Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Cutter Laboratories, Inc.
- Product code
- Product code ELW
- Device class
- Class 2
- Regulation
- 21 CFR 872.3660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Berkeley, CA, US
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