DESERET EPIDURAL CATHETER— 510(k) K834472

Substantially Equivalent

Parke-Davis Co.

FDA 510(k) clearance K834472 for DESERET EPIDURAL CATHETER, Substantially Equivalent on 1984-01-13. Applicant: Parke-Davis Co..

Clearance details

Applicant: Parke-Davis Co.
Advisory panel: Unknown
Date received: 1983-12-20
Decision date: 1984-01-13
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.