THERAPAX DXT 300 MODEL HF-300— 510(k) K973315

Substantially Equivalent

Pantak, Inc.

FDA 510(k) clearance K973315 for THERAPAX DXT 300 MODEL HF-300, Substantially Equivalent on 1997-12-02. Applicant: Pantak, Inc.. Device class: 2.

Clearance details

Applicant: Pantak, Inc.
Product code: Code JAD
Device class: Class 2
Regulation: 21 CFR 892.5900
Advisory panel: Radiology
Date received: 1997-09-03
Decision date: 1997-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branford, CT, 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.