THERATRON 1000— 510(k) K894165

Substantially Equivalent

Theratronics, Inc.

FDA 510(k) clearance K894165 for THERATRON 1000, Substantially Equivalent on 1990-02-01. Applicant: Theratronics, Inc.. Device class: 2.

Clearance details

Applicant: Theratronics, Inc.
Product code: Code IWB
Device class: Class 2
Regulation: 21 CFR 892.5750
Advisory panel: Radiology
Date received: 1989-06-16
Decision date: 1990-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kanata, Ontario, Canada, CA

Download summary PDF View on FDA.gov ↗

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More clearances from Theratronics, Inc.

K983917 — THERATRON ELITE1998-12-04
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K964607 — THERATON 1000E1997-05-28
K954679 — THERAPLAN PLUS1996-11-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.