Cleared Traditional

K950288 - AUTOLASER MULTI FORMAT CAMERA

K950288 is the FDA 510(k) clearance for AUTOLASER MULTI FORMAT CAMERA by Afp Imaging Corp.. It is a Class 2 Radiology device (product code LMC) cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K950288 · Afp Imaging Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1995
Decision
69d
Days
Class 2
Risk

K950288 is an FDA 510(k) clearance for the AUTOLASER MULTI FORMAT CAMERA. Classified as Camera, Multi Format, Radiological (product code LMC), Class II - Special Controls.

Submitted by Afp Imaging Corp. (Elmsford, US). The FDA issued a Cleared decision on April 4, 1995 after a review of 69 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2040 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Afp Imaging Corp. devices

Submission Details

510(k) Number K950288 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1995
Decision Date April 04, 1995
Days to Decision 69 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 107d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LMC Camera, Multi Format, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2040
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 - LMC Camera, Multi Format, Radiological

All 34
Devices cleared under the same product code (LMC) and FDA review panel - the closest regulatory comparables to K950288.
SIENET TELERADIOLOGY PRODUCT LINE
K955394 · Siemens Medical Solutions USA, Inc. · Feb 1996
FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L
K950721 · Fujifilm Medical System U.S.A., Inc. · May 1995
FIKO FO
K950610 · Fujifilm Medical System U.S.A., Inc. · Apr 1995
FUJI MEDICAL LASER IMAGER FL-IM D
K945475 · Fujifilm Medical System U.S.A., Inc. · Mar 1995
PMI100 VIDEO IMAGER
K925220 · Heraeus Kulzer, Inc. · May 1993
PHILIPS LASER DISK ARCHIVE
K923481 · Philips Medical Systems, Inc. · May 1993