Cleared Traditional

K923112 - ANGIO-BAND

K923112 is the FDA 510(k) clearance for ANGIO-BAND by Cook, Inc.. It is a Class 2 Radiology device (product code IZI) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K923112 · Cook, Inc. · Radiology device
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Sep 1992
Decision
90d
Days
Class 2
Risk

K923112 is an FDA 510(k) clearance for the ANGIO-BAND. Classified as System, X-ray, Angiographic (product code IZI), Class II - Special Controls.

Submitted by Cook, Inc. (Ontario L4a 7x5, CA). The FDA issued a Cleared decision on September 23, 1992 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1600 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Cook, Inc. devices

Submission Details

510(k) Number K923112 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 1992
Decision Date September 23, 1992
Days to Decision 90 days
Submission Type Traditional
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
17d faster than avg
Panel avg: 107d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IZI System, X-ray, Angiographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1600
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 - IZI System, X-ray, Angiographic

All 97
Devices cleared under the same product code (IZI) and FDA review panel - the closest regulatory comparables to K923112.
CSP-A (CEILING SUSPENDED POSITIONER-ANGIO)
K924137 · Fischer Imaging Corp. · Dec 1992
ANGIOGRAPHIC X-RAY SYSTEM
K922222 · Siemens Medical Solutions USA, Inc. · Dec 1992
PHILIPS INTEGRIS V3000 ROTATIONAL ANGIO FUNCTION
K923813 · Philips Medical Systems, Inc. · Oct 1992
AWOS ANGIOGRAPHIC WORKSTATION
K922804 · Siemens Medical Solutions USA, Inc. · Aug 1992
PHILIPS CARDIAC WORKSTATION
K922622 · Philips Medical Systems, Inc. · Aug 1992
PHILIPS INTEGRIS V3000 FILM
K921101 · Philips Medical Systems, Inc. · May 1992