LUMISYS DICOM TOOKLIT— 510(k) K953371

Substantially Equivalent

Lumisys, Inc.

FDA 510(k) clearance K953371 for LUMISYS DICOM TOOKLIT, Substantially Equivalent on 1995-10-18. Applicant: Lumisys, Inc.. Device class: 1.

Clearance details

Applicant: Lumisys, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-07-18
Decision date: 1995-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Lumisys, Inc.

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K933129 — LUMISCAN 501993-10-07
K902347 — COMPACT LASER IMAGER, MODEL CLI-1001991-03-04

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