HEMORRELIEF DEVICE— 510(k) K973590

Name: FDA 510(k) clearance K973590
Creator: U.S. Food and Drug Administration
Published: 1998-02-05

Substantially Equivalent

A.Stein - Regulatory Affairs Consulting

FDA 510(k) clearance K973590 for HEMORRELIEF DEVICE, Substantially Equivalent on 1998-02-05. Applicant: A.Stein - Regulatory Affairs Consulting. Device class: Unclassified.

Clearance details

Applicant: A.Stein - Regulatory Affairs Consulting
Product code: Code LKX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1997-09-22
Decision date: 1998-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ginot Shomron 44853, IL

Download summary PDF View on FDA.gov ↗

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