DYNASORB— 510(k) K951561

Substantially Equivalent

Dermarx Corp.

FDA 510(k) clearance K951561 for DYNASORB, Substantially Equivalent on 1995-09-01. Applicant: Dermarx Corp.. Device class: 1.

Clearance details

Applicant: Dermarx Corp.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1995-04-05
Decision date: 1995-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, 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.