LOCKETT MEDICAL CORP. GAUZE— 510(k) K950404

Name: FDA 510(k) clearance K950404
Creator: U.S. Food and Drug Administration
Published: 1995-04-17

Substantially Equivalent

Lockett Medical Corp.

FDA 510(k) clearance K950404 for LOCKETT MEDICAL CORP. GAUZE, Substantially Equivalent on 1995-04-17. Applicant: Lockett Medical Corp.. Device class: Unclassified.

Clearance details

Applicant: Lockett Medical Corp.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-01-31
Decision date: 1995-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Providence, RI, 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.