Cleared Traditional

K896615 - CINE CAMERA CONTROL MODEL PK2037

K896615 is the FDA 510(k) clearance for CINE CAMERA CONTROL MODEL PK2037 by Perkins Mfg. Co.. It is a Class 2 Radiology device (product code IZJ) cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K896615 · Perkins Mfg. Co. · Radiology device
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Jan 1990
Decision
44d
Days
Class 2
Risk

K896615 is an FDA 510(k) clearance for the CINE CAMERA CONTROL MODEL PK2037. Classified as Camera, X-ray, Fluorographic, Cine Or Spot (product code IZJ), Class II - Special Controls.

Submitted by Perkins Mfg. Co. (Dallas, US). The FDA issued a Cleared decision on January 4, 1990 after a review of 44 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1620 - 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 K896615 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 1989
Decision Date January 04, 1990
Days to Decision 44 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 107d · This submission: 44d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IZJ Camera, X-ray, Fluorographic, Cine Or Spot
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1620
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 - IZJ Camera, X-ray, Fluorographic, Cine Or Spot

Devices cleared under the same product code (IZJ) and FDA review panel - the closest regulatory comparables to K896615.
DSP OPTION
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