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

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..

Clearance details

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

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