MICROPREP CAVITY PREPERATION SYSTEM— 510(k) K932997

Name: FDA 510(k) clearance K932997
Creator: U.S. Food and Drug Administration
Published: 1994-04-25

Substantially Equivalent

Sunrise Technologies, Inc.

FDA 510(k) clearance K932997 for MICROPREP CAVITY PREPERATION SYSTEM, Substantially Equivalent on 1994-04-25. Applicant: Sunrise Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Sunrise Technologies, Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1993-06-18
Decision date: 1994-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fremont, 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.