MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE— 510(k) K911099

Name: FDA 510(k) clearance K911099
Creator: U.S. Food and Drug Administration
Published: 1991-06-25

Substantially Equivalent

Pilling Co.

FDA 510(k) clearance K911099 for MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE, Substantially Equivalent on 1991-06-25. Applicant: Pilling Co.. Device class: 2.

Clearance details

Applicant: Pilling Co.
Product code: Code DWX
Device class: Class 2
Regulation: 21 CFR 870.4875
Advisory panel: Cardiovascular
Date received: 1991-03-12
Decision date: 1991-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Washington, PA, US

Download summary PDF View on FDA.gov ↗

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