CILCO ASCAN— 510(k) K827371

Substantially Equivalent

Cilco, Inc.

FDA 510(k) clearance K827371 for CILCO ASCAN, Substantially Equivalent on 1982-07-09. Applicant: Cilco, Inc..

Clearance details

Applicant: Cilco, Inc.
Advisory panel: Unknown
Date received: 1982-03-29
Decision date: 1982-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Huntington, WV, US

Download summary PDF View on FDA.gov ↗

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