Cleared Traditional

K892934 - 1 VIDEO TAPE RECORDER MODEL BK-224 H

K892934 is the FDA 510(k) clearance for 1 VIDEO TAPE RECORDER MODEL BK-224 H by Perkins Mfg. Co.. It is a Class 2 Radiology device (product code OXO) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K892934 · Perkins Mfg. Co. · Radiology device
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Jul 1989
Decision
90d
Days
Class 2
Risk

K892934 is an FDA 510(k) clearance for the 1 VIDEO TAPE RECORDER MODEL BK-224 H. Classified as Image-intensified Fluoroscopic X-ray System, Mobile (product code OXO), Class II - Special Controls.

Submitted by Perkins Mfg. Co. (Dallas, US). The FDA issued a Cleared decision on July 20, 1989 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 892.1650 - 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 Perkins Mfg. Co. devices

Submission Details

510(k) Number K892934 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 21, 1989
Decision Date July 20, 1989
Days to Decision 90 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
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 OXO Image-intensified Fluoroscopic X-ray System, Mobile
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Fluoroscopy Of The Human Body.
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 - OXO Image-intensified Fluoroscopic X-ray System, Mobile

All 33
Devices cleared under the same product code (OXO) and FDA review panel - the closest regulatory comparables to K892934.
MOBILE X-RAY SYSTEM
K913525 · Siemens Medical Solutions USA, Inc. · Oct 1991
PHILIPS BV-29 IMAGING SYSTEM
K910115 · Philips Medical Systems, Inc. · Feb 1991
SXT-60F/60M MOBILE C ARM X-RAY UNIT
K896387 · Toshiba America Medical Systems, In.C · Feb 1990
MOBILE C-ARM OMNI 325
K880518 · Fischer Imaging Corp. · Mar 1988
FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS.
K760429 · Varian Assoc., Inc. · Aug 1976