DUAL FLEX NON-LATEX— 510(k) K905026

Substantially Equivalent

Mmi, Inc.

FDA 510(k) clearance K905026 for DUAL FLEX NON-LATEX, Substantially Equivalent on 1991-12-18. Applicant: Mmi, Inc.. Device class: 2.

Clearance details

Applicant: Mmi, Inc.
Product code: Code FGD
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1990-11-07
Decision date: 1991-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southfield, MI, 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.