KREATIV MODEL KV-1— 510(k) K940776

Substantially Equivalent

Kreativ, Inc.

FDA 510(k) clearance K940776 for KREATIV MODEL KV-1, Substantially Equivalent on 1994-12-21. Applicant: Kreativ, Inc.. Device class: 2.

Clearance details

Applicant: Kreativ, Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1994-02-22
Decision date: 1994-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vancouver, WA, 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.