ACCU-PREP— 510(k) K970484

Substantially Equivalent

Bisco, Inc.

FDA 510(k) clearance K970484 for ACCU-PREP, Substantially Equivalent on 1997-07-01. Applicant: Bisco, Inc.. Device class: 2.

Clearance details

Applicant: Bisco, Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1997-02-10
Decision date: 1997-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Itasca, IL, 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.