DYNASTY U1-33 AGM— 510(k) K942311

Substantially Equivalent

Foley & Lardner

FDA 510(k) clearance K942311 for DYNASTY U1-33 AGM, Substantially Equivalent on 1994-11-07. Applicant: Foley & Lardner. Device class: 1.

Clearance details

Applicant: Foley & Lardner
Product code: Code KNN
Device class: Class 1
Regulation: 21 CFR 890.3920
Advisory panel: Physical Medicine
Date received: 1994-05-13
Decision date: 1994-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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