K-FLEX— 510(k) K811519

Substantially Equivalent

Sybron 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
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Data sourced from openFDA. This site is unofficial and independent of the FDA.