FERTICARE PERSONAL THERAPEUTIC VIBRATOR— 510(k) K955589

Name: FDA 510(k) clearance K955589
Creator: U.S. Food and Drug Administration
Published: 1996-04-11

Substantially Equivalent

Multicept, Aps.

FDA 510(k) clearance K955589 for FERTICARE PERSONAL THERAPEUTIC VIBRATOR, Substantially Equivalent on 1996-04-11. Applicant: Multicept, Aps.. Device class: 2.

Clearance details

Applicant: Multicept, Aps.
Product code: Code KXQ
Device class: Class 2
Regulation: 21 CFR 884.5960
Advisory panel: Obstetrics/Gynecology
Date received: 1995-12-07
Decision date: 1996-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 2960 Rungsted Kyst,Denmark, DK

Download summary PDF View on FDA.gov ↗

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