K-FLEX— 510(k) K811519
Substantially EquivalentSybron Corp.
FDA 510(k) clearance K811519 for K-FLEX, Substantially Equivalent on 1981-06-26. Applicant: Sybron Corp..
Clearance details
- Applicant
- Sybron Corp.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.