TRIMODE SP DENTAL INTRA ORAL X-RAY— 510(k) K896963

Name: FDA 510(k) clearance K896963
Creator: U.S. Food and Drug Administration
Published: 1990-01-22

Substantially Equivalent

Tempo Technology, Inc.

FDA 510(k) clearance K896963 for TRIMODE SP DENTAL INTRA ORAL X-RAY, Substantially Equivalent on 1990-01-22. Applicant: Tempo Technology, Inc.. Device class: 2.

Clearance details

Applicant: Tempo Technology, Inc.
Product code: Code EAP
Device class: Class 2
Regulation: 21 CFR 872.1810
Advisory panel: Dental
Date received: 1989-12-15
Decision date: 1990-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia City, IN, US

Download summary PDF View on FDA.gov ↗

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