DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM— 510(k) K880322

Name: FDA 510(k) clearance K880322
Creator: U.S. Food and Drug Administration
Published: 1988-07-13

Substantially Equivalent

Dentronix, Inc.

FDA 510(k) clearance K880322 for DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM, Substantially Equivalent on 1988-07-13. Applicant: Dentronix, Inc.. Device class: 2.

Clearance details

Applicant: Dentronix, Inc.
Product code: Code KMH
Device class: Class 2
Regulation: 21 CFR 880.6870
Advisory panel: General Hospital
Date received: 1988-01-27
Decision date: 1988-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ivyland, PA, US

Download summary PDF View on FDA.gov ↗

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