SEMINOR— 510(k) K905764

Substantially Equivalent

Promedex, Inc.

FDA 510(k) clearance K905764 for SEMINOR, Substantially Equivalent on 1991-03-12. Applicant: Promedex, Inc.. Device class: 2.

Clearance details

Applicant: Promedex, Inc.
Product code: Code MFD
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1990-12-27
Decision date: 1991-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Woth, TX, US

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More clearances from Promedex, Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.