NOVADERM— 510(k) K896531

Substantially Equivalent

Syncare Corp.

FDA 510(k) clearance K896531 for NOVADERM, Substantially Equivalent on 1990-04-13. Applicant: Syncare Corp.. Device class: 1.

Clearance details

Applicant: Syncare Corp.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1989-11-16
Decision date: 1990-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Charleston, SC, 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.