Cleared Traditional

K827609 - MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY (FDA 510(k) Clearance)

K827609 · Midwest X-Ray Equipment Co. · Radiology device
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Jul 1982
Decision
31d
Days
-
Risk

K827609 is an FDA 510(k) clearance for the MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY.

Submitted by Midwest X-Ray Equipment Co. (Aurora, US). The FDA issued a Cleared decision on July 9, 1982 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel. 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 Midwest X-Ray Equipment Co. devices

Submission Details

510(k) Number K827609 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1982
Decision Date July 09, 1982
Days to Decision 31 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 107d · This submission: 31d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -