MAXILL-AIR SINUS VENTILATION TUBE— 510(k) K813474

Substantially Equivalent

Xomed, Inc.

FDA 510(k) clearance K813474 for MAXILL-AIR SINUS VENTILATION TUBE, Substantially Equivalent on 1982-01-12. Applicant: Xomed, Inc.. Device class: 1.

Clearance details

Applicant: Xomed, Inc.
Product code: Code KAM
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-12-01
Decision date: 1982-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arnold, MO, 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.