NUVO BARRIER FILM— 510(k) K980117

Substantially Equivalent

Biomedical Development Co.

FDA 510(k) clearance K980117 for NUVO BARRIER FILM, Substantially Equivalent on 1998-12-18. Applicant: Biomedical Development Co.. Device class: 1.

Clearance details

Applicant: Biomedical Development Co.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1998-01-13
Decision date: 1998-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, 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.