WOUNDFOAM 4 X 4— 510(k) K953070

Substantially Equivalent

Trinity Laboratories, Inc.

FDA 510(k) clearance K953070 for WOUNDFOAM 4 X 4, Substantially Equivalent on 1995-09-08. Applicant: Trinity Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Trinity Laboratories, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1995-06-30
Decision date: 1995-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salisbury, MD, US

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