PELVICFLEXER EXERCISE DEVICE— 510(k) K011688

Substantially Equivalent

Pelvicflex, Inc.

FDA 510(k) clearance K011688 for PELVICFLEXER EXERCISE DEVICE, Substantially Equivalent on 2002-03-20. Applicant: Pelvicflex, Inc.. Device class: 2.

Clearance details

Applicant: Pelvicflex, Inc.
Product code: Code HIR
Device class: Class 2
Regulation: 21 CFR 884.1425
Advisory panel: Obstetrics/Gynecology
Date received: 2001-05-31
Decision date: 2002-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, 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.