PLEASURE PLUS— 510(k) K902772

Substantially Equivalent

Medimix Products, Inc.

FDA 510(k) clearance K902772 for PLEASURE PLUS, Substantially Equivalent on 1991-08-14. Applicant: Medimix Products, Inc.. Device class: 2.

Clearance details

Applicant: Medimix Products, Inc.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1990-06-22
Decision date: 1991-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.