HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS— 510(k) K855150

Name: FDA 510(k) clearance K855150
Creator: U.S. Food and Drug Administration
Published: 1986-04-01

Substantially Equivalent

Hpk International, Inc.

FDA 510(k) clearance K855150 for HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS, Substantially Equivalent on 1986-04-01. Applicant: Hpk International, Inc.. Device class: Unclassified.

Clearance details

Applicant: Hpk International, Inc.
Product code: Code LKX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1985-12-26
Decision date: 1986-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.