QUALITONE ULTRA CANAL GENESIS— 510(k) K904730

Substantially Equivalent

Qualitone

FDA 510(k) clearance K904730 for QUALITONE ULTRA CANAL GENESIS, Substantially Equivalent on 1990-12-07. Applicant: Qualitone. Device class: 1.

Clearance details

Applicant: Qualitone
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1990-10-17
Decision date: 1990-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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More clearances from Qualitone

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Data sourced from openFDA. This site is unofficial and independent of the FDA.