HOWTEK 960— 510(k) K970908

Substantially Equivalent

Howtek, Inc.

FDA 510(k) clearance K970908 for HOWTEK 960, Substantially Equivalent on 1997-05-20. 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: 1997-03-11
Decision date: 1997-05-20
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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K953117 — SCANMASTER DX1996-01-18

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