MILEX KEGEL PERINEAL EXERCISER— 510(k) K862410

Name: FDA 510(k) clearance K862410
Creator: U.S. Food and Drug Administration
Published: 1986-07-31

Substantially Equivalent

Milex Products, Inc.

FDA 510(k) clearance K862410 for MILEX KEGEL PERINEAL EXERCISER, Substantially Equivalent on 1986-07-31. Applicant: Milex Products, Inc.. Device class: 2.

Clearance details

Applicant: Milex Products, Inc.
Product code: Code HIR
Device class: Class 2
Regulation: 21 CFR 884.1425
Advisory panel: Obstetrics/Gynecology
Date received: 1986-06-25
Decision date: 1986-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.