MEDI-KLEER— 510(k) K904871

Substantially Equivalent

North American Marketing Corp.

FDA 510(k) clearance K904871 for MEDI-KLEER, Substantially Equivalent on 1991-09-17. Applicant: North American Marketing Corp.. Device class: 2.

Clearance details

Applicant: North American Marketing Corp.
Product code: Code OCT
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1990-10-29
Decision date: 1991-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ynez, CA, 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.