ESTILUX POSTERIOR XR— 510(k) K813568

Substantially Equivalent

Kulzer, Inc.

FDA 510(k) clearance K813568 for ESTILUX POSTERIOR XR, Substantially Equivalent on 1982-01-29. Applicant: Kulzer, Inc..

Clearance details

Applicant: Kulzer, Inc.
Product code: Code EBF
Advisory panel: Dental
Date received: 1981-12-22
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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