Cleared Traditional

K970349 - FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667

K970349 is an FDA 510(k) clearance for FUJI MEDICAL LASER IMAGER MF PRINT SERV..., manufactured by Fujifilm Medical System U.S.A., Inc.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K970349 · Fujifilm Medical System U.S.A., Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1997
Decision
60d
Days
Class 2
Risk

K970349 is an FDA 510(k) clearance for the FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Fujifilm Medical System U.S.A., Inc. (Stamford, US). The FDA issued a Cleared decision on March 31, 1997 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Incremental AI imaging tool. Moderate equivalence dependency. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Fujifilm Medical System U.S.A., Inc. devices

FDA 510(k) Submission Details - K970349

510(k) Number K970349 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 1997
Decision Date March 31, 1997
Days to Decision 60 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 107d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LLZ Device Classification - Class 2, Special Controls

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 1881
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K970349.
DOWNSCAN 120
K970451 · Merlin Engineering Works, Inc. · Apr 1997
PICTURE ARCHIVING & COMMUNICATIONS DEVICE
K970534 · Multimedia Solutions · Apr 1997
UPSCAN 120
K970450 · Merlin Engineering Works, Inc. · Apr 1997
DOCTORS REVIEW SYSTEM
K970402 · Digisonics, Inc. · Mar 1997
EPI-SCOPE OPTION FOR Q SERIES CT SYSTEMS
K962010 · Philips Medical Systems (Cleveland), Inc. · Mar 1997
DIGITAL IMAGE ANALYSIS SYSTEM
K962153 · University of Washington · Jan 1997