Cleared Traditional

UNION BROACH BLEACHING LIGHT (K852474) - FDA 510(k) Clearance

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1985
Decision
20d
Days
-
Risk

K852474 is an FDA 510(k) clearance for the UNION BROACH BLEACHING LIGHT.

Submitted by Union Broach, Div. Moyco Industries, Inc. (New York, US). The FDA issued a Cleared decision on July 1, 1985 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Dental 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 Union Broach, Div. Moyco Industries, Inc. devices

Submission Details

510(k) Number K852474 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 11, 1985
Decision Date July 01, 1985
Days to Decision 20 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
107d faster than avg
Panel avg: 127d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -