ULTRAFLOW— 510(k) K871901

Substantially Equivalent

Custom Industries, Inc.

FDA 510(k) clearance K871901 for ULTRAFLOW, Substantially Equivalent on 1987-06-01. Applicant: Custom Industries, Inc.. Device class: 2.

Clearance details

Applicant: Custom Industries, Inc.
Product code: Code FZH
Device class: Class 2
Regulation: 21 CFR 878.5070
Advisory panel: General, Plastic Surgery
Date received: 1987-05-15
Decision date: 1987-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greensboro, NC, 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.