HANCOCK AORTIC PUNCH— 510(k) K800122

Substantially Equivalent

Hancock Laboratories, Inc.

FDA 510(k) clearance K800122 for HANCOCK AORTIC PUNCH, Substantially Equivalent on 1980-02-01. Applicant: Hancock Laboratories, Inc..

Clearance details

Applicant: Hancock Laboratories, Inc.
Product code: Code DWS
Advisory panel: Cardiovascular
Date received: 1980-01-18
Decision date: 1980-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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