Cleared Traditional

K915232 - GRUNDIG ELECTRONICS VARIOUS MODELS

K915232 is the FDA 510(k) clearance for GRUNDIG ELECTRONICS VARIOUS MODELS by Perkins Mfg. Co.. It is a Class 2 Radiology device (product code IZI) cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K915232 · Perkins Mfg. Co. · Radiology device
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Jan 1992
Decision
48d
Days
Class 2
Risk

K915232 is an FDA 510(k) clearance for the GRUNDIG ELECTRONICS VARIOUS MODELS. Classified as System, X-ray, Angiographic (product code IZI), Class II - Special Controls.

Submitted by Perkins Mfg. Co. (Dallas, US). The FDA issued a Cleared decision on January 9, 1992 after a review of 48 days - a notably fast clearance cycle.

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: 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 Perkins Mfg. Co. devices

Submission Details

510(k) Number K915232 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 22, 1991
Decision Date January 09, 1992
Days to Decision 48 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 107d · This submission: 48d
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 100
Devices cleared under the same product code (IZI) and FDA review panel - the closest regulatory comparables to K915232.
POLYTRON DIGITAL IMAGING SYSTEM
K920705 · Siemens Medical Solutions USA, Inc. · Apr 1992
DXS DIGITAL X-RAY SUBTRACTION
K914376 · Philips Medical Systems (Cleveland), Inc. · Feb 1992
STORZ IMAGING SYSTEM
K915199 · Fischer Imaging Corp. · Jan 1992
HICOR
K914313 · Siemens Gammasonics, Inc. · Nov 1991
ADVANCE DISPOSABLE CONTROL SYRINGE
K911732 · Advance Medical Designs, Inc. · Sep 1991
POLYSTAR ANGIOGRAPHIC X-RAY SYSTEM
K913120 · Siemens Medical Solutions USA, Inc. · Aug 1991