Cleared Traditional

DELTA PLAN II RADIATION THERAPY PLANNING SYSTEM (K827122) - FDA 510(k) Clearance

K827122 · Technicare Corp. · Radiology device
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Mar 1982
Decision
54d
Days
-
Risk

K827122 is an FDA 510(k) clearance for the DELTA PLAN II RADIATION THERAPY PLANNING SYSTEM.

Submitted by Technicare Corp. (Solon, US). The FDA issued a Cleared decision on March 31, 1982 after a review of 54 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 Technicare Corp. devices

Submission Details

510(k) Number K827122 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 1982
Decision Date March 31, 1982
Days to Decision 54 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 107d · This submission: 54d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -