SCANMASTER DX— 510(k) K953117

Substantially Equivalent

Howtek, Inc.

FDA 510(k) clearance K953117 for SCANMASTER DX, Substantially Equivalent on 1996-01-18. Applicant: Howtek, Inc.. Device class: 2.

Clearance details

Applicant: Howtek, Inc.
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1995-07-03
Decision date: 1996-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hudson, NH, US

Download summary PDF View on FDA.gov ↗

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More clearances from Howtek, Inc.

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K970908 — HOWTEK 9601997-05-20

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