TELICAM— 510(k) K980474

Name: FDA 510(k) clearance K980474
Creator: U.S. Food and Drug Administration
Published: 1998-04-13

Substantially Equivalent

Dental/Medical Diagnostic Systems, Inc.

FDA 510(k) clearance K980474 for TELICAM, Substantially Equivalent on 1998-04-13. Applicant: Dental/Medical Diagnostic Systems, Inc.. Device class: 1.

Clearance details

Applicant: Dental/Medical Diagnostic Systems, Inc.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1998-02-06
Decision date: 1998-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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