Cleared Abbreviated

K090578 - SHIMADZU COLLIMATOR R-30H

K090578 is the FDA 510(k) clearance for SHIMADZU COLLIMATOR R-30H by Shimadzu Corp.. It is a Class 2 Radiology device (product code IZW) cleared through the Abbreviated 510(k) pathway after a 248-day FDA review.

K090578 · Shimadzu Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2009
Decision
248d
Days
Class 2
Risk

K090578 is an FDA 510(k) clearance for the SHIMADZU COLLIMATOR R-30H. Classified as Collimator, Automatic, Radiographic (product code IZW), Class II - Special Controls.

Submitted by Shimadzu Corp. (Torrance, US). The FDA issued a Cleared decision on November 6, 2009 after a review of 248 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1610 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Shimadzu Corp. devices

Submission Details

510(k) Number K090578 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 03, 2009
Decision Date November 06, 2009
Days to Decision 248 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
141d slower than avg
Panel avg: 107d · This submission: 248d
Pathway characteristics
Standards-based clearance path.

Device Classification

Product Code IZW Collimator, Automatic, Radiographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1610
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 - IZW Collimator, Automatic, Radiographic

All 7
Devices cleared under the same product code (IZW) and FDA review panel - the closest regulatory comparables to K090578.
SHIMADZU COLLIMATOR R-300
K101039 · Shimadzu Corp. · Sep 2010
PHILIPS NICOL COLLIMATOR FAMILY
K990423 · Philips Medical Systems, Inc. · Mar 1999
PHILIPS GALLILEO AUTOMATIC COLLIMATOR (OR BEAM LIMITING DEVICE)
K951372 · Philips Medical Systems, Inc. · May 1995
COLLIMATOR F-20
K920725 · Shimadzu Medical Systems · Apr 1992
STEREO COLLIMATOR RF-T SERIES
K920733 · Shimadzu Medical Systems · Apr 1992
COLLIMASTER-90
K911127 · Varian Assoc., Inc. · Sep 1991