THE STRIPPER— 510(k) K993699

Substantially Equivalent

Mid-Atlantic Diagnostics, Inc.

FDA 510(k) clearance K993699 for THE STRIPPER, Substantially Equivalent on 2000-05-16. Applicant: Mid-Atlantic Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Mid-Atlantic Diagnostics, Inc.
Product code: Code MQH
Device class: Class 2
Regulation: 21 CFR 884.6130
Advisory panel: Obstetrics/Gynecology
Date received: 1999-11-02
Decision date: 2000-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medford, NJ, US

Download summary PDF View on FDA.gov ↗

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