THE ADDITION— 510(k) K102683

Substantially Equivalent

Ob The-Addition, LLC

FDA 510(k) clearance K102683 for THE ADDITION, Substantially Equivalent on 2011-01-06. Applicant: Ob The-Addition, LLC. Device class: 2.

Clearance details

Applicant: Ob The-Addition, LLC
Product code: Code MUI
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 2010-09-17
Decision date: 2011-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, 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.