ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033— 510(k) K992032

Name: FDA 510(k) clearance K992032
Creator: U.S. Food and Drug Administration
Published: 1999-08-19

Substantially Equivalent

Acrymed, Inc.

FDA 510(k) clearance K992032 for ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033, Substantially Equivalent on 1999-08-19. Applicant: Acrymed, Inc.. Device class: 1.

Clearance details

Applicant: Acrymed, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1999-06-16
Decision date: 1999-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, 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.